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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.

rs6703700

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:13620091 (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 / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.366750 (97075/264690, TOPMED)
A=0.347183 (84907/244560, ALFA)
A=0.360573 (50481/140002, GnomAD) (+ 19 more)
A=0.37118 (29209/78692, PAGE_STUDY)
A=0.41645 (11768/28258, 14KJPN)
A=0.41975 (7035/16760, 8.3KJPN)
A=0.3888 (2490/6404, 1000G_30x)
A=0.3930 (1968/5008, 1000G)
A=0.3025 (1355/4480, Estonian)
A=0.3622 (1396/3854, ALSPAC)
A=0.3401 (1261/3708, TWINSUK)
A=0.3563 (1044/2930, KOREAN)
A=0.3581 (656/1832, Korea1K)
A=0.358 (357/998, GoNL)
A=0.403 (310/770, PRJEB37584)
A=0.333 (200/600, NorthernSweden)
A=0.350 (112/320, HapMap)
G=0.361 (109/302, SGDP_PRJ)
A=0.333 (72/216, Qatari)
A=0.453 (97/214, Vietnamese)
A=0.35 (14/40, GENOME_DK)
G=0.45 (10/22, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
Publications
0 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 249596 G=0.652627 A=0.347373
European Sub 220566 G=0.654357 A=0.345643
African Sub 7964 G=0.5951 A=0.4049
African Others Sub 316 G=0.535 A=0.465
African American Sub 7648 G=0.5975 A=0.4025
Asian Sub 3832 G=0.6156 A=0.3844
East Asian Sub 3102 G=0.6231 A=0.3769
Other Asian Sub 730 G=0.584 A=0.416
Latin American 1 Sub 1024 G=0.6445 A=0.3555
Latin American 2 Sub 6554 G=0.6930 A=0.3070
South Asian Sub 366 G=0.511 A=0.489
Other Sub 9290 G=0.6541 A=0.3459


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=0.633250 A=0.366750
Allele Frequency Aggregator Total Global 244560 G=0.652817 A=0.347183
Allele Frequency Aggregator European Sub 217472 G=0.654250 A=0.345750
Allele Frequency Aggregator Other Sub 8490 G=0.6561 A=0.3439
Allele Frequency Aggregator African Sub 6822 G=0.5943 A=0.4057
Allele Frequency Aggregator Latin American 2 Sub 6554 G=0.6930 A=0.3070
Allele Frequency Aggregator Asian Sub 3832 G=0.6156 A=0.3844
Allele Frequency Aggregator Latin American 1 Sub 1024 G=0.6445 A=0.3555
Allele Frequency Aggregator South Asian Sub 366 G=0.511 A=0.489
gnomAD - Genomes Global Study-wide 140002 G=0.639427 A=0.360573
gnomAD - Genomes European Sub 75828 G=0.66460 A=0.33540
gnomAD - Genomes African Sub 41936 G=0.58916 A=0.41084
gnomAD - Genomes American Sub 13642 G=0.65855 A=0.34145
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=0.6528 A=0.3472
gnomAD - Genomes East Asian Sub 3120 G=0.6099 A=0.3901
gnomAD - Genomes Other Sub 2152 G=0.6329 A=0.3671
The PAGE Study Global Study-wide 78692 G=0.62882 A=0.37118
The PAGE Study AfricanAmerican Sub 32512 G=0.59277 A=0.40723
The PAGE Study Mexican Sub 10810 G=0.70583 A=0.29417
The PAGE Study Asian Sub 8318 G=0.5786 A=0.4214
The PAGE Study PuertoRican Sub 7918 G=0.6562 A=0.3438
The PAGE Study NativeHawaiian Sub 4532 G=0.6924 A=0.3076
The PAGE Study Cuban Sub 4226 G=0.6628 A=0.3372
The PAGE Study Dominican Sub 3828 G=0.6293 A=0.3707
The PAGE Study CentralAmerican Sub 2450 G=0.6641 A=0.3359
The PAGE Study SouthAmerican Sub 1982 G=0.6640 A=0.3360
The PAGE Study NativeAmerican Sub 1260 G=0.6643 A=0.3357
The PAGE Study SouthAsian Sub 856 G=0.519 A=0.481
14KJPN JAPANESE Study-wide 28258 G=0.58355 A=0.41645
8.3KJPN JAPANESE Study-wide 16760 G=0.58025 A=0.41975
1000Genomes_30x Global Study-wide 6404 G=0.6112 A=0.3888
1000Genomes_30x African Sub 1786 G=0.6053 A=0.3947
1000Genomes_30x Europe Sub 1266 G=0.6785 A=0.3215
1000Genomes_30x South Asian Sub 1202 G=0.5258 A=0.4742
1000Genomes_30x East Asian Sub 1170 G=0.5889 A=0.4111
1000Genomes_30x American Sub 980 G=0.666 A=0.334
1000Genomes Global Study-wide 5008 G=0.6070 A=0.3930
1000Genomes African Sub 1322 G=0.6006 A=0.3994
1000Genomes East Asian Sub 1008 G=0.5863 A=0.4137
1000Genomes Europe Sub 1006 G=0.6809 A=0.3191
1000Genomes South Asian Sub 978 G=0.521 A=0.479
1000Genomes American Sub 694 G=0.663 A=0.337
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.6975 A=0.3025
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.6378 A=0.3622
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.6599 A=0.3401
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.6437 A=0.3563, T=0.0000
Korean Genome Project KOREAN Study-wide 1832 G=0.6419 A=0.3581
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.642 A=0.358
CNV burdens in cranial meningiomas Global Study-wide 770 G=0.597 A=0.403
CNV burdens in cranial meningiomas CRM Sub 770 G=0.597 A=0.403
Northern Sweden ACPOP Study-wide 600 G=0.667 A=0.333
HapMap Global Study-wide 320 G=0.650 A=0.350
HapMap American Sub 120 G=0.658 A=0.342
HapMap African Sub 110 G=0.636 A=0.364
HapMap Asian Sub 90 G=0.66 A=0.34
SGDP_PRJ Global Study-wide 302 G=0.361 A=0.639
Qatari Global Study-wide 216 G=0.667 A=0.333
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.547 A=0.453
The Danish reference pan genome Danish Study-wide 40 G=0.65 A=0.35
Siberian Global Study-wide 22 G=0.45 A=0.55
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 1 NC_000001.11:g.13620091G>A
GRCh38.p14 chr 1 NC_000001.11:g.13620091G>T
GRCh37.p13 chr 1 NC_000001.10:g.13946586G>A
GRCh37.p13 chr 1 NC_000001.10:g.13946586G>T
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 T
GRCh38.p14 chr 1 NC_000001.11:g.13620091= NC_000001.11:g.13620091G>A NC_000001.11:g.13620091G>T
GRCh37.p13 chr 1 NC_000001.10:g.13946586= NC_000001.10:g.13946586G>A NC_000001.10:g.13946586G>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#.

110 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss9904970 Jul 11, 2003 (116)
2 PERLEGEN ss23155149 Sep 20, 2004 (123)
3 ABI ss44023498 Mar 14, 2006 (126)
4 PERLEGEN ss68758902 May 18, 2007 (127)
5 HGSV ss85084430 Dec 15, 2007 (130)
6 BCMHGSC_JDW ss87234166 Mar 23, 2008 (129)
7 BGI ss102720933 Dec 01, 2009 (131)
8 1000GENOMES ss107999934 Jan 22, 2009 (130)
9 1000GENOMES ss110074748 Jan 24, 2009 (130)
10 ILLUMINA-UK ss118506059 Feb 14, 2009 (130)
11 ILLUMINA ss160799987 Dec 01, 2009 (131)
12 ENSEMBL ss161166679 Dec 01, 2009 (131)
13 COMPLETE_GENOMICS ss163089530 Jul 04, 2010 (132)
14 COMPLETE_GENOMICS ss163847566 Jul 04, 2010 (132)
15 BUSHMAN ss198039530 Jul 04, 2010 (132)
16 1000GENOMES ss218243483 Jul 14, 2010 (132)
17 1000GENOMES ss230431637 Jul 14, 2010 (132)
18 1000GENOMES ss238146220 Jul 15, 2010 (132)
19 GMI ss275720918 May 04, 2012 (137)
20 ILLUMINA ss481323753 May 04, 2012 (137)
21 ILLUMINA ss481348954 May 04, 2012 (137)
22 ILLUMINA ss482330190 Sep 08, 2015 (146)
23 ILLUMINA ss485457006 May 04, 2012 (137)
24 ILLUMINA ss537380885 Sep 08, 2015 (146)
25 TISHKOFF ss553812422 Apr 25, 2013 (138)
26 SSMP ss647587272 Apr 25, 2013 (138)
27 ILLUMINA ss778577084 Sep 08, 2015 (146)
28 ILLUMINA ss783173980 Sep 08, 2015 (146)
29 ILLUMINA ss784129446 Sep 08, 2015 (146)
30 ILLUMINA ss832433550 Sep 08, 2015 (146)
31 ILLUMINA ss834034169 Sep 08, 2015 (146)
32 EVA-GONL ss974871185 Aug 21, 2014 (142)
33 JMKIDD_LAB ss1067679665 Aug 21, 2014 (142)
34 1000GENOMES ss1289745679 Aug 21, 2014 (142)
35 DDI ss1425717690 Apr 01, 2015 (144)
36 EVA_GENOME_DK ss1573896323 Apr 01, 2015 (144)
37 EVA_DECODE ss1584228356 Apr 01, 2015 (144)
38 EVA_UK10K_ALSPAC ss1599576811 Apr 01, 2015 (144)
39 EVA_UK10K_TWINSUK ss1642570844 Apr 01, 2015 (144)
40 ILLUMINA ss1751868158 Sep 08, 2015 (146)
41 HAMMER_LAB ss1793928018 Sep 08, 2015 (146)
42 WEILL_CORNELL_DGM ss1918073801 Feb 12, 2016 (147)
43 ILLUMINA ss1945985226 Feb 12, 2016 (147)
44 ILLUMINA ss1958242997 Feb 12, 2016 (147)
45 GENOMED ss1966687410 Jul 19, 2016 (147)
46 JJLAB ss2019550345 Sep 14, 2016 (149)
47 USC_VALOUEV ss2147548604 Dec 20, 2016 (150)
48 HUMAN_LONGEVITY ss2160164010 Dec 20, 2016 (150)
49 ILLUMINA ss2632479397 Nov 08, 2017 (151)
50 GRF ss2697449315 Nov 08, 2017 (151)
51 ILLUMINA ss2710666103 Nov 08, 2017 (151)
52 GNOMAD ss2751820972 Nov 08, 2017 (151)
53 SWEGEN ss2986333274 Nov 08, 2017 (151)
54 ILLUMINA ss3021056145 Nov 08, 2017 (151)
55 BIOINF_KMB_FNS_UNIBA ss3023538598 Nov 08, 2017 (151)
56 CSHL ss3343326373 Nov 08, 2017 (151)
57 ILLUMINA ss3625525608 Oct 11, 2018 (152)
58 ILLUMINA ss3626029840 Oct 11, 2018 (152)
59 ILLUMINA ss3630517657 Oct 11, 2018 (152)
60 ILLUMINA ss3632881313 Oct 11, 2018 (152)
61 ILLUMINA ss3633575186 Oct 11, 2018 (152)
62 ILLUMINA ss3634307782 Oct 11, 2018 (152)
63 ILLUMINA ss3635269290 Oct 11, 2018 (152)
64 ILLUMINA ss3635983966 Oct 11, 2018 (152)
65 ILLUMINA ss3637019664 Oct 11, 2018 (152)
66 ILLUMINA ss3640015146 Oct 11, 2018 (152)
67 ILLUMINA ss3644481064 Oct 11, 2018 (152)
68 ILLUMINA ss3651380268 Oct 11, 2018 (152)
69 EGCUT_WGS ss3654419654 Jul 12, 2019 (153)
70 EVA_DECODE ss3686197241 Jul 12, 2019 (153)
71 ILLUMINA ss3724997883 Jul 12, 2019 (153)
72 ACPOP ss3726804677 Jul 12, 2019 (153)
73 ILLUMINA ss3744042144 Jul 12, 2019 (153)
74 ILLUMINA ss3744608753 Jul 12, 2019 (153)
75 EVA ss3745848072 Jul 12, 2019 (153)
76 PAGE_CC ss3770786665 Jul 12, 2019 (153)
77 ILLUMINA ss3772110358 Jul 12, 2019 (153)
78 PACBIO ss3783328531 Jul 12, 2019 (153)
79 PACBIO ss3789002108 Jul 12, 2019 (153)
80 PACBIO ss3793874819 Jul 12, 2019 (153)
81 KHV_HUMAN_GENOMES ss3798869377 Jul 12, 2019 (153)
82 EVA ss3826030668 Apr 25, 2020 (154)
83 EVA ss3836402700 Apr 25, 2020 (154)
84 EVA ss3841806787 Apr 25, 2020 (154)
85 SGDP_PRJ ss3848242153 Apr 25, 2020 (154)
86 KRGDB ss3893132744 Apr 25, 2020 (154)
87 KOGIC ss3943865824 Apr 25, 2020 (154)
88 EVA ss3984452405 Apr 25, 2021 (155)
89 EVA ss4016894182 Apr 25, 2021 (155)
90 TOPMED ss4439759992 Apr 25, 2021 (155)
91 TOMMO_GENOMICS ss5142569722 Apr 25, 2021 (155)
92 EVA ss5237260341 Apr 25, 2021 (155)
93 1000G_HIGH_COVERAGE ss5241245823 Oct 12, 2022 (156)
94 EVA ss5314594085 Oct 12, 2022 (156)
95 EVA ss5316864164 Oct 12, 2022 (156)
96 HUGCELL_USP ss5442430588 Oct 12, 2022 (156)
97 EVA ss5505768739 Oct 12, 2022 (156)
98 1000G_HIGH_COVERAGE ss5513033236 Oct 12, 2022 (156)
99 SANFORD_IMAGENETICS ss5624196938 Oct 12, 2022 (156)
100 SANFORD_IMAGENETICS ss5624962871 Oct 12, 2022 (156)
101 TOMMO_GENOMICS ss5666906986 Oct 12, 2022 (156)
102 EVA ss5799475501 Oct 12, 2022 (156)
103 YY_MCH ss5800342509 Oct 12, 2022 (156)
104 EVA ss5831562876 Oct 12, 2022 (156)
105 EVA ss5847526194 Oct 12, 2022 (156)
106 EVA ss5848790369 Oct 12, 2022 (156)
107 EVA ss5907105935 Oct 12, 2022 (156)
108 EVA ss5936781807 Oct 12, 2022 (156)
109 EVA ss5979263561 Oct 12, 2022 (156)
110 EVA ss5979934674 Oct 12, 2022 (156)
111 1000Genomes NC_000001.10 - 13946586 Oct 11, 2018 (152)
112 1000Genomes_30x NC_000001.11 - 13620091 Oct 12, 2022 (156)
113 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 13946586 Oct 11, 2018 (152)
114 Genetic variation in the Estonian population NC_000001.10 - 13946586 Oct 11, 2018 (152)
115 The Danish reference pan genome NC_000001.10 - 13946586 Apr 25, 2020 (154)
116 gnomAD - Genomes NC_000001.11 - 13620091 Apr 25, 2021 (155)
117 Genome of the Netherlands Release 5 NC_000001.10 - 13946586 Apr 25, 2020 (154)
118 HapMap NC_000001.11 - 13620091 Apr 25, 2020 (154)
119 KOREAN population from KRGDB NC_000001.10 - 13946586 Apr 25, 2020 (154)
120 Korean Genome Project NC_000001.11 - 13620091 Apr 25, 2020 (154)
121 Northern Sweden NC_000001.10 - 13946586 Jul 12, 2019 (153)
122 The PAGE Study NC_000001.11 - 13620091 Jul 12, 2019 (153)
123 CNV burdens in cranial meningiomas NC_000001.10 - 13946586 Apr 25, 2021 (155)
124 Qatari NC_000001.10 - 13946586 Apr 25, 2020 (154)
125 SGDP_PRJ NC_000001.10 - 13946586 Apr 25, 2020 (154)
126 Siberian NC_000001.10 - 13946586 Apr 25, 2020 (154)
127 8.3KJPN NC_000001.10 - 13946586 Apr 25, 2021 (155)
128 14KJPN NC_000001.11 - 13620091 Oct 12, 2022 (156)
129 TopMed NC_000001.11 - 13620091 Apr 25, 2021 (155)
130 UK 10K study - Twins NC_000001.10 - 13946586 Oct 11, 2018 (152)
131 A Vietnamese Genetic Variation Database NC_000001.10 - 13946586 Jul 12, 2019 (153)
132 ALFA NC_000001.11 - 13620091 Apr 25, 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)
rs59676600 May 25, 2008 (130)
rs386604505 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss85084430 NC_000001.8:13691891:G:A NC_000001.11:13620090:G:A (self)
ss87234166, ss107999934, ss110074748, ss118506059, ss163089530, ss163847566, ss198039530, ss275720918, ss481323753, ss1584228356 NC_000001.9:13819172:G:A NC_000001.11:13620090:G:A (self)
423768, 218369, 157902, 1395845, 94260, 310138, 89542, 1707, 115731, 259133, 64958, 539029, 218369, 45751, ss218243483, ss230431637, ss238146220, ss481348954, ss482330190, ss485457006, ss537380885, ss553812422, ss647587272, ss778577084, ss783173980, ss784129446, ss832433550, ss834034169, ss974871185, ss1067679665, ss1289745679, ss1425717690, ss1573896323, ss1599576811, ss1642570844, ss1751868158, ss1793928018, ss1918073801, ss1945985226, ss1958242997, ss1966687410, ss2019550345, ss2147548604, ss2632479397, ss2697449315, ss2710666103, ss2751820972, ss2986333274, ss3021056145, ss3343326373, ss3625525608, ss3626029840, ss3630517657, ss3632881313, ss3633575186, ss3634307782, ss3635269290, ss3635983966, ss3637019664, ss3640015146, ss3644481064, ss3651380268, ss3654419654, ss3726804677, ss3744042144, ss3744608753, ss3745848072, ss3772110358, ss3783328531, ss3789002108, ss3793874819, ss3826030668, ss3836402700, ss3848242153, ss3893132744, ss3984452405, ss4016894182, ss5142569722, ss5237260341, ss5314594085, ss5316864164, ss5505768739, ss5624196938, ss5624962871, ss5799475501, ss5831562876, ss5847526194, ss5936781807, ss5979263561, ss5979934674 NC_000001.10:13946585:G:A NC_000001.11:13620090:G:A (self)
559171, 2989568, 15802, 243825, 8134, 744090, 3366327, 16271414497, ss2160164010, ss3023538598, ss3686197241, ss3724997883, ss3770786665, ss3798869377, ss3841806787, ss3943865824, ss4439759992, ss5241245823, ss5442430588, ss5513033236, ss5666906986, ss5800342509, ss5848790369, ss5907105935 NC_000001.11:13620090:G:A NC_000001.11:13620090:G:A (self)
ss23155149, ss44023498, ss68758902, ss102720933, ss160799987, ss161166679 NT_004610.19:626673:G:A NC_000001.11:13620090:G:A (self)
ss9904970 NT_004873.14:323750:G:A NC_000001.11:13620090:G:A (self)
310138, ss3893132744 NC_000001.10:13946585:G:T NC_000001.11:13620090:G:T (self)
Help

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

No publications for rs6703700

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