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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs4728709

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr7:87604286 (GRCh38.p14) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
G>A
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.172209 (45582/264690, TOPMED)
A=0.081638 (17108/209558, ALFA)
A=0.165292 (23121/139880, GnomAD) (+ 20 more)
A=0.16954 (4791/28258, 14KJPN)
A=0.16780 (2812/16758, 8.3KJPN)
A=0.1797 (1151/6404, 1000G_30x)
A=0.1769 (886/5008, 1000G)
A=0.0692 (310/4480, Estonian)
A=0.0623 (240/3854, ALSPAC)
A=0.0636 (236/3708, TWINSUK)
A=0.1683 (493/2930, KOREAN)
A=0.1430 (298/2084, HGDP_Stanford)
A=0.2087 (394/1888, HapMap)
A=0.1534 (281/1832, Korea1K)
A=0.063 (63/998, GoNL)
A=0.152 (120/790, PRJEB37584)
A=0.147 (92/626, Chileans)
A=0.040 (24/600, NorthernSweden)
A=0.125 (27/216, Qatari)
G=0.396 (57/144, SGDP_PRJ)
A=0.00 (0/56, Ancient Sardinia)
A=0.07 (3/40, GENOME_DK)
G=0.2 (1/4, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ABCB1 : Intron Variant
Publications
7 citations
Genomic View
See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 209558 G=0.918362 A=0.081638
European Sub 178648 G=0.933640 A=0.066360
African Sub 7748 G=0.6336 A=0.3664
African Others Sub 274 G=0.489 A=0.511
African American Sub 7474 G=0.6389 A=0.3611
Asian Sub 748 G=0.849 A=0.151
East Asian Sub 572 G=0.857 A=0.143
Other Asian Sub 176 G=0.824 A=0.176
Latin American 1 Sub 982 G=0.848 A=0.152
Latin American 2 Sub 9036 G=0.8807 A=0.1193
South Asian Sub 5054 G=0.9432 A=0.0568
Other Sub 7342 G=0.8928 A=0.1072


Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
TopMed Global Study-wide 264690 G=0.827791 A=0.172209
Allele Frequency Aggregator Total Global 209558 G=0.918362 A=0.081638
Allele Frequency Aggregator European Sub 178648 G=0.933640 A=0.066360
Allele Frequency Aggregator Latin American 2 Sub 9036 G=0.8807 A=0.1193
Allele Frequency Aggregator African Sub 7748 G=0.6336 A=0.3664
Allele Frequency Aggregator Other Sub 7342 G=0.8928 A=0.1072
Allele Frequency Aggregator South Asian Sub 5054 G=0.9432 A=0.0568
Allele Frequency Aggregator Latin American 1 Sub 982 G=0.848 A=0.152
Allele Frequency Aggregator Asian Sub 748 G=0.849 A=0.151
gnomAD - Genomes Global Study-wide 139880 G=0.834708 A=0.165292
gnomAD - Genomes European Sub 75836 G=0.93168 A=0.06832
gnomAD - Genomes African Sub 41818 G=0.63002 A=0.36998
gnomAD - Genomes American Sub 13642 G=0.88975 A=0.11025
gnomAD - Genomes Ashkenazi Jewish Sub 3316 G=0.9403 A=0.0597
gnomAD - Genomes East Asian Sub 3122 G=0.8671 A=0.1329
gnomAD - Genomes Other Sub 2146 G=0.8364 A=0.1636
14KJPN JAPANESE Study-wide 28258 G=0.83046 A=0.16954
8.3KJPN JAPANESE Study-wide 16758 G=0.83220 A=0.16780
1000Genomes_30x Global Study-wide 6404 G=0.8203 A=0.1797
1000Genomes_30x African Sub 1786 G=0.6081 A=0.3919
1000Genomes_30x Europe Sub 1266 G=0.9423 A=0.0577
1000Genomes_30x South Asian Sub 1202 G=0.9268 A=0.0732
1000Genomes_30x East Asian Sub 1170 G=0.8726 A=0.1274
1000Genomes_30x American Sub 980 G=0.856 A=0.144
1000Genomes Global Study-wide 5008 G=0.8231 A=0.1769
1000Genomes African Sub 1322 G=0.5930 A=0.4070
1000Genomes East Asian Sub 1008 G=0.8700 A=0.1300
1000Genomes Europe Sub 1006 G=0.9394 A=0.0606
1000Genomes South Asian Sub 978 G=0.940 A=0.060
1000Genomes American Sub 694 G=0.860 A=0.140
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.9308 A=0.0692
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.9377 A=0.0623
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.9364 A=0.0636
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.8317 A=0.1683
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.8570 A=0.1430
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.860 A=0.140
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.920 A=0.080
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.891 A=0.109
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.950 A=0.050
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.496 A=0.504
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.926 A=0.074
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.90 A=0.10
HapMap Global Study-wide 1888 G=0.7913 A=0.2087
HapMap American Sub 768 G=0.896 A=0.104
HapMap African Sub 692 G=0.613 A=0.387
HapMap Asian Sub 252 G=0.877 A=0.123
HapMap Europe Sub 176 G=0.915 A=0.085
Korean Genome Project KOREAN Study-wide 1832 G=0.8466 A=0.1534
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.937 A=0.063
CNV burdens in cranial meningiomas Global Study-wide 790 G=0.848 A=0.152
CNV burdens in cranial meningiomas CRM Sub 790 G=0.848 A=0.152
Chileans Chilean Study-wide 626 G=0.853 A=0.147
Northern Sweden ACPOP Study-wide 600 G=0.960 A=0.040
Qatari Global Study-wide 216 G=0.875 A=0.125
SGDP_PRJ Global Study-wide 144 G=0.396 A=0.604
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 56 G=1.00 A=0.00
The Danish reference pan genome Danish Study-wide 40 G=0.93 A=0.07
Siberian Global Study-wide 4 G=0.2 A=0.8
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 7 NC_000007.14:g.87604286G>A
GRCh37.p13 chr 7 NC_000007.13:g.87233602G>A
ABCB1 RefSeqGene NG_011513.1:g.113963C>T
Gene: ABCB1, ATP binding cassette subfamily B member 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ABCB1 transcript variant 3 NM_000927.5:c.-330-3208C>T N/A Intron Variant
ABCB1 transcript variant 2 NM_001348944.2:c.-183-320…

NM_001348944.2:c.-183-3208C>T

 		N/A Intron Variant
ABCB1 transcript variant 1 NM_001348945.2:c.-154-114…

NM_001348945.2:c.-154-1146C>T

 		N/A Intron Variant
ABCB1 transcript variant 4 NM_001348946.2:c. N/A Genic Upstream Transcript Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement G= A
GRCh38.p14 chr 7 NC_000007.14:g.87604286= NC_000007.14:g.87604286G>A
GRCh37.p13 chr 7 NC_000007.13:g.87233602= NC_000007.13:g.87233602G>A
ABCB1 RefSeqGene NG_011513.1:g.113963= NG_011513.1:g.113963C>T
ABCB1 transcript variant 3 NM_000927.4:c.-330-3208= NM_000927.4:c.-330-3208C>T
ABCB1 transcript variant 3 NM_000927.5:c.-330-3208= NM_000927.5:c.-330-3208C>T
ABCB1 transcript variant 2 NM_001348944.2:c.-183-3208= NM_001348944.2:c.-183-3208C>T
ABCB1 transcript variant 1 NM_001348945.2:c.-154-1146= NM_001348945.2:c.-154-1146C>T
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

106 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 WI_SSAHASNP ss6517547 Feb 20, 2003 (111)
2 WUGSC_SSAHASNP ss14580455 Dec 05, 2003 (120)
3 PERLEGEN ss23548765 Sep 20, 2004 (123)
4 AFFY ss66519377 Nov 29, 2006 (127)
5 ILLUMINA ss67366037 Nov 29, 2006 (127)
6 ILLUMINA ss67750742 Nov 29, 2006 (127)
7 ILLUMINA ss68234645 Dec 12, 2006 (127)
8 ILLUMINA ss70819626 May 23, 2008 (130)
9 ILLUMINA ss71400950 May 16, 2007 (127)
10 ILLUMINA ss75522851 Dec 06, 2007 (129)
11 AFFY ss76341965 Dec 08, 2007 (130)
12 ILLUMINA ss79312362 Dec 14, 2007 (130)
13 KRIBB_YJKIM ss84331804 Dec 14, 2007 (130)
14 HGSV ss84718513 Dec 14, 2007 (130)
15 ILLUMINA-UK ss116181538 Feb 14, 2009 (130)
16 ILLUMINA ss123088073 Dec 01, 2009 (131)
17 ILLUMINA ss154311587 Dec 01, 2009 (131)
18 ILLUMINA ss159488280 Dec 01, 2009 (131)
19 ILLUMINA ss160703677 Dec 01, 2009 (131)
20 ILLUMINA ss171884458 Jul 04, 2010 (132)
21 AFFY ss173322922 Jul 04, 2010 (132)
22 ILLUMINA ss173792508 Jul 04, 2010 (132)
23 BUSHMAN ss203607860 Jul 04, 2010 (132)
24 1000GENOMES ss223188250 Jul 14, 2010 (132)
25 1000GENOMES ss234064171 Jul 15, 2010 (132)
26 1000GENOMES ss241002123 Jul 15, 2010 (132)
27 GMI ss279426175 May 04, 2012 (137)
28 PJP ss293911002 May 09, 2011 (134)
29 ILLUMINA ss481021313 May 04, 2012 (137)
30 ILLUMINA ss481042324 May 04, 2012 (137)
31 ILLUMINA ss482029030 Sep 08, 2015 (146)
32 ILLUMINA ss485305669 May 04, 2012 (137)
33 ILLUMINA ss537264821 Sep 08, 2015 (146)
34 TISHKOFF ss560135094 Apr 25, 2013 (138)
35 SSMP ss654534161 Apr 25, 2013 (138)
36 ILLUMINA ss778916418 Sep 08, 2015 (146)
37 ILLUMINA ss783098663 Sep 08, 2015 (146)
38 ILLUMINA ss784055946 Sep 08, 2015 (146)
39 ILLUMINA ss825642880 Apr 01, 2015 (144)
40 ILLUMINA ss832357213 Sep 08, 2015 (146)
41 ILLUMINA ss832999689 Jul 13, 2019 (153)
42 ILLUMINA ss834377812 Sep 08, 2015 (146)
43 EVA-GONL ss984507572 Aug 21, 2014 (142)
44 JMKIDD_LAB ss1074771992 Aug 21, 2014 (142)
45 1000GENOMES ss1326016493 Aug 21, 2014 (142)
46 EVA_GENOME_DK ss1582294344 Apr 01, 2015 (144)
47 EVA_DECODE ss1594083466 Apr 01, 2015 (144)
48 EVA_UK10K_ALSPAC ss1618631865 Apr 01, 2015 (144)
49 EVA_UK10K_TWINSUK ss1661625898 Apr 01, 2015 (144)
50 EVA_SVP ss1712968875 Apr 01, 2015 (144)
51 ILLUMINA ss1752698270 Sep 08, 2015 (146)
52 HAMMER_LAB ss1805098743 Sep 08, 2015 (146)
53 WEILL_CORNELL_DGM ss1927770681 Feb 12, 2016 (147)
54 JJLAB ss2024567752 Sep 14, 2016 (149)
55 USC_VALOUEV ss2152788478 Dec 20, 2016 (150)
56 HUMAN_LONGEVITY ss2295536337 Dec 20, 2016 (150)
57 SYSTEMSBIOZJU ss2626775341 Nov 08, 2017 (151)
58 ILLUMINA ss2634629050 Nov 08, 2017 (151)
59 ILLUMINA ss2635174057 Nov 08, 2017 (151)
60 GRF ss2708493148 Nov 08, 2017 (151)
61 GNOMAD ss2855822076 Nov 08, 2017 (151)
62 SWEGEN ss3001578506 Nov 08, 2017 (151)
63 BIOINF_KMB_FNS_UNIBA ss3026077327 Nov 08, 2017 (151)
64 ILLUMINA ss3629856673 Oct 12, 2018 (152)
65 ILLUMINA ss3632535219 Oct 12, 2018 (152)
66 ILLUMINA ss3633469351 Oct 12, 2018 (152)
67 ILLUMINA ss3634194588 Oct 12, 2018 (152)
68 ILLUMINA ss3635129107 Oct 12, 2018 (152)
69 ILLUMINA ss3635874238 Oct 12, 2018 (152)
70 ILLUMINA ss3636862558 Oct 12, 2018 (152)
71 ILLUMINA ss3637627239 Oct 12, 2018 (152)
72 ILLUMINA ss3638708348 Oct 12, 2018 (152)
73 ILLUMINA ss3639356362 Oct 12, 2018 (152)
74 ILLUMINA ss3639972783 Oct 12, 2018 (152)
75 ILLUMINA ss3640836399 Oct 12, 2018 (152)
76 ILLUMINA ss3643643428 Oct 12, 2018 (152)
77 ILLUMINA ss3644016799 Oct 12, 2018 (152)
78 EGCUT_WGS ss3669332014 Jul 13, 2019 (153)
79 EVA_DECODE ss3720147255 Jul 13, 2019 (153)
80 ACPOP ss3734834876 Jul 13, 2019 (153)
81 ILLUMINA ss3745429124 Jul 13, 2019 (153)
82 EVA ss3766829226 Jul 13, 2019 (153)
83 ILLUMINA ss3772922027 Jul 13, 2019 (153)
84 KHV_HUMAN_GENOMES ss3810002701 Jul 13, 2019 (153)
85 HGDP ss3847882748 Apr 26, 2020 (154)
86 SGDP_PRJ ss3867817406 Apr 26, 2020 (154)
87 KRGDB ss3915078121 Apr 26, 2020 (154)
88 KOGIC ss3962029403 Apr 26, 2020 (154)
89 EVA ss3984591265 Apr 26, 2021 (155)
90 EVA ss3985306939 Apr 26, 2021 (155)
91 EVA ss4017345605 Apr 26, 2021 (155)
92 TOPMED ss4753657442 Apr 26, 2021 (155)
93 TOMMO_GENOMICS ss5184289684 Apr 26, 2021 (155)
94 1000G_HIGH_COVERAGE ss5273748880 Oct 16, 2022 (156)
95 EVA ss5315261563 Oct 16, 2022 (156)
96 EVA ss5374984557 Oct 16, 2022 (156)
97 HUGCELL_USP ss5470747982 Oct 16, 2022 (156)
98 EVA ss5509036802 Oct 16, 2022 (156)
99 1000G_HIGH_COVERAGE ss5562380687 Oct 16, 2022 (156)
100 SANFORD_IMAGENETICS ss5643429620 Oct 16, 2022 (156)
101 TOMMO_GENOMICS ss5724888390 Oct 16, 2022 (156)
102 EVA ss5799729871 Oct 16, 2022 (156)
103 YY_MCH ss5808857143 Oct 16, 2022 (156)
104 EVA ss5823148476 Oct 16, 2022 (156)
105 EVA ss5859765559 Oct 16, 2022 (156)
106 EVA ss5972606479 Oct 16, 2022 (156)
107 1000Genomes NC_000007.13 - 87233602 Oct 12, 2018 (152)
108 1000Genomes_30x NC_000007.14 - 87604286 Oct 16, 2022 (156)
109 The Avon Longitudinal Study of Parents and Children NC_000007.13 - 87233602 Oct 12, 2018 (152)
110 Chileans NC_000007.13 - 87233602 Apr 26, 2020 (154)
111 Genetic variation in the Estonian population NC_000007.13 - 87233602 Oct 12, 2018 (152)
112 The Danish reference pan genome NC_000007.13 - 87233602 Apr 26, 2020 (154)
113 gnomAD - Genomes NC_000007.14 - 87604286 Apr 26, 2021 (155)
114 Genome of the Netherlands Release 5 NC_000007.13 - 87233602 Apr 26, 2020 (154)
115 HGDP-CEPH-db Supplement 1 NC_000007.12 - 87071538 Apr 26, 2020 (154)
116 HapMap NC_000007.14 - 87604286 Apr 26, 2020 (154)
117 KOREAN population from KRGDB NC_000007.13 - 87233602 Apr 26, 2020 (154)
118 Korean Genome Project NC_000007.14 - 87604286 Apr 26, 2020 (154)
119 Northern Sweden NC_000007.13 - 87233602 Jul 13, 2019 (153)
120 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000007.13 - 87233602 Apr 26, 2021 (155)
121 CNV burdens in cranial meningiomas NC_000007.13 - 87233602 Apr 26, 2021 (155)
122 Qatari NC_000007.13 - 87233602 Apr 26, 2020 (154)
123 SGDP_PRJ NC_000007.13 - 87233602 Apr 26, 2020 (154)
124 Siberian NC_000007.13 - 87233602 Apr 26, 2020 (154)
125 8.3KJPN NC_000007.13 - 87233602 Apr 26, 2021 (155)
126 14KJPN NC_000007.14 - 87604286 Oct 16, 2022 (156)
127 TopMed NC_000007.14 - 87604286 Apr 26, 2021 (155)
128 UK 10K study - Twins NC_000007.13 - 87233602 Oct 12, 2018 (152)
129 ALFA NC_000007.14 - 87604286 Apr 26, 2021 (155)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID History Updated (Build)
rs10374943 Feb 27, 2004 (120)
rs56490249 May 23, 2008 (130)
rs56710587 May 23, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss84718513, ss3639356362, ss3639972783, ss3644016799 NC_000007.11:86878252:G:A NC_000007.14:87604285:G:A (self)
560640, ss66519377, ss76341965, ss116181538, ss173322922, ss203607860, ss279426175, ss293911002, ss481021313, ss825642880, ss1594083466, ss1712968875, ss2635174057, ss3643643428, ss3847882748 NC_000007.12:87071537:G:A NC_000007.14:87604285:G:A (self)
38018531, 21156070, 413771, 15070262, 8459283, 9446820, 22255515, 8119741, 532866, 140690, 9812611, 19834386, 5304832, 42258991, 21156070, ss223188250, ss234064171, ss241002123, ss481042324, ss482029030, ss485305669, ss537264821, ss560135094, ss654534161, ss778916418, ss783098663, ss784055946, ss832357213, ss832999689, ss834377812, ss984507572, ss1074771992, ss1326016493, ss1582294344, ss1618631865, ss1661625898, ss1752698270, ss1805098743, ss1927770681, ss2024567752, ss2152788478, ss2626775341, ss2634629050, ss2708493148, ss2855822076, ss3001578506, ss3629856673, ss3632535219, ss3633469351, ss3634194588, ss3635129107, ss3635874238, ss3636862558, ss3637627239, ss3638708348, ss3640836399, ss3669332014, ss3734834876, ss3745429124, ss3766829226, ss3772922027, ss3867817406, ss3915078121, ss3984591265, ss3985306939, ss4017345605, ss5184289684, ss5315261563, ss5374984557, ss5509036802, ss5643429620, ss5799729871, ss5823148476, ss5972606479 NC_000007.13:87233601:G:A NC_000007.14:87604285:G:A (self)
49906622, 268220672, 3438624, 18407404, 58725494, 591035001, 10769319207, ss2295536337, ss3026077327, ss3720147255, ss3810002701, ss3962029403, ss4753657442, ss5273748880, ss5470747982, ss5562380687, ss5724888390, ss5808857143, ss5859765559 NC_000007.14:87604285:G:A NC_000007.14:87604285:G:A (self)
ss14580455 NT_007933.13:12467817:G:A NC_000007.14:87604285:G:A (self)
ss6517547, ss23548765, ss67366037, ss67750742, ss68234645, ss70819626, ss71400950, ss75522851, ss79312362, ss84331804, ss123088073, ss154311587, ss159488280, ss160703677, ss171884458, ss173792508 NT_007933.15:25266444:G:A NC_000007.14:87604285:G:A (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

7 citations for rs4728709
PMID Title Author Year Journal
19107762 Genetic susceptibility of lung cancer associated with common variants in the 3' untranslated regions of the adenosine triphosphate-binding cassette B1 (ABCB1) and ABCC1 candidate transporter genes for carcinogen export. Wang H et al. 2009 Cancer
21686133 Polymorphisms in ABCB1 and ERCC2 associated with ovarian cancer outcome. Peethambaram P et al. 2011 International journal of molecular epidemiology and genetics
21712189 Analysis of pharmacogenetic traits in two distinct South African populations. Ikediobi O et al. 2011 Human genomics
24434428 Host genetic variants of ABCB1 and IL15 influence treatment outcome in paediatric acute lymphoblastic leukaemia. Lu Y et al. 2014 British journal of cancer
27904761 Vincristine-induced peripheral neuropathy in pediatric cancer patients. Mora E et al. 2016 American journal of cancer research
35158880 Pharmacogenomics of Vincristine-Induced Peripheral Neuropathy in Children with Cancer: A Systematic Review and Meta-Analysis. Uittenboogaard A et al. 2022 Cancers
35316848 Population Pharmacokinetics of Rivaroxaban in Chinese Patients with Non-Valvular Atrial Fibrillation: A Prospective Multicenter Study. Zhang F et al. 2022 Clinical pharmacokinetics
Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top▲ Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post761+d5e8e07