OR5T3 - SNP

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Select item 79397741.

rs7939774 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C,G [Show Flanks]
Chromosome:: 11:56251985 (GRCh38)
11:56019461 (GRCh37)
Canonical SPDI:: NC_000011.10:56251984:T:A,NC_000011.10:56251984:T:C,NC_000011.10:56251984:T:G
Gene:: OR5T3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.321544/5955 (ALFA)
T=0.12963/28 (Vietnamese)
T=0.166667/88 (SGDP_PRJ)
T=0.188396/552 (KOREAN)
T=0.207764/3482 (TOMMO)
T=0.236571/1185 (1000Genomes)
T=0.263889/57 (Qatari)
T=0.288462/15 (Siberian)
T=0.3/12 (GENOME_DK)
T=0.305391/42709 (GnomAD)
T=0.306649/81167 (TOPMED)
T=0.328333/197 (NorthernSweden)
T=0.334598/1499 (Estonian)
T=0.335761/1245 (TWINSUK)
T=0.347691/1340 (ALSPAC)
T=0.492986/492 (GoNL)
HGVS:: NC_000011.10:g.56251985T>A, NC_000011.10:g.56251985T>C, NC_000011.10:g.56251985T>G, NC_000011.9:g.56019461T>A, NC_000011.9:g.56019461T>C, NC_000011.9:g.56019461T>G, NW_025791793.1:g.62734T>A, NW_025791793.1:g.62734T>C, NW_025791793.1:g.62734T>G, NW_003871073.1:g.62734T>A, NW_003871073.1:g.62734T>C, NW_003871073.1:g.62734T>G

Select item 107918972.

rs10791897 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 11:56250398 (GRCh38)
11:56017874 (GRCh37)
Canonical SPDI:: NC_000011.10:56250397:A:C,NC_000011.10:56250397:A:G,NC_000011.10:56250397:A:T
Gene:: OR5T3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.135045/2551 (ALFA)
C=0./0 (KOREAN)
A=0.000106/2 (TOMMO)
A=0.054152/30 (SGDP_PRJ)
A=0.094316/472 (1000Genomes)
A=0.102204/102 (GoNL)
A=0.11/66 (NorthernSweden)
A=0.123508/476 (ALSPAC)
A=0.130798/485 (TWINSUK)
A=0.140881/19676 (GnomAD)
A=0.141573/37473 (TOPMED)
A=0.142857/8 (Siberian)
A=0.15/6 (GENOME_DK)
A=0.175926/38 (Qatari)
HGVS:: NC_000011.10:g.56250398A>C, NC_000011.10:g.56250398A>G, NC_000011.10:g.56250398A>T, NC_000011.9:g.56017874A>C, NC_000011.9:g.56017874A>G, NC_000011.9:g.56017874A>T, NW_025791793.1:g.61147A>C, NW_025791793.1:g.61147A>G, NW_025791793.1:g.61147A>T, NW_003871073.1:g.61147A>C, NW_003871073.1:g.61147A>G, NW_003871073.1:g.61147A>T

Select item 108961433.

rs10896143 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:56250432 (GRCh38)
11:56017908 (GRCh37)
Canonical SPDI:: NC_000011.10:56250431:T:A,NC_000011.10:56250431:T:C
Gene:: OR5T3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.460464/29804 (ALFA)
T=0.256818/113 (SGDP_PRJ)
T=0.306604/65 (Vietnamese)
T=0.317406/930 (KOREAN)
T=0.339421/5688 (TOMMO)
C=0.375/15 (GENOME_DK)
T=0.428571/18 (Siberian)
C=0.430861/60149 (GnomAD)
C=0.433333/260 (NorthernSweden)
C=0.440372/116562 (TOPMED)
C=0.441619/1702 (ALSPAC)
C=0.448214/2008 (Estonian)
C=0.456311/1692 (TWINSUK)
C=0.466667/154 (HapMap)
T=0.467593/101 (Qatari)
C=0.468938/468 (GoNL)
T=0.488913/2448 (1000Genomes)
HGVS:: NC_000011.10:g.56250432T>A, NC_000011.10:g.56250432T>C, NC_000011.9:g.56017908T>A, NC_000011.9:g.56017908T>C, NW_025791793.1:g.61181T>A, NW_025791793.1:g.61181T>C, NW_003871073.1:g.61181T>A, NW_003871073.1:g.61181T>C

Select item 112276384.

rs11227638 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:56252109 (GRCh38)
11:56019585 (GRCh37)
Canonical SPDI:: NC_000011.10:56252108:A:T
Gene:: OR5T3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.109317/2065 (ALFA)
T=0.083333/18 (Qatari)
T=0.086142/46 (MGP)
T=0.093939/31 (HapMap)
T=0.096294/25488 (TOPMED)
T=0.099469/498 (1000Genomes)
T=0.104277/14595 (GnomAD)
T=0.115179/516 (Estonian)
T=0.128328/376 (KOREAN)
T=0.128438/495 (ALSPAC)
T=0.131573/2205 (TOMMO)
T=0.131877/489 (TWINSUK)
T=0.139279/139 (GoNL)
T=0.143333/86 (NorthernSweden)
T=0.172897/37 (Vietnamese)
T=0.25/10 (GENOME_DK)
A=0.453704/49 (SGDP_PRJ)
A=0.5/7 (Siberian)
HGVS:: NC_000011.10:g.56252109A>T, NC_000011.9:g.56019585A>T, NW_025791793.1:g.62858A>T, NW_003871073.1:g.62858A>T

PubMed

Select item 112276405.

rs11227640 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:56252194 (GRCh38)
11:56019670 (GRCh37)
Canonical SPDI:: NC_000011.10:56252193:A:G,NC_000011.10:56252193:A:T
Gene:: OR5T3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000077/2 (ALFA)
T=0./0 (HapMap)
T=0.000193/27 (GnomAD)
T=0.000342/1 (KOREAN)
T=0.000343/76 (GnomAD_exomes)
T=0.000349/38 (ExAC)
T=0.000937/5 (1000Genomes)
T=0.004673/1 (Vietnamese)
A=0.5/2 (SGDP_PRJ)
HGVS:: NC_000011.10:g.56252194A>G, NC_000011.10:g.56252194A>T, NC_000011.9:g.56019670A>G, NC_000011.9:g.56019670A>T, NW_025791793.1:g.62943A>G, NW_025791793.1:g.62943A>T, NW_003871073.1:g.62943A>G, NW_003871073.1:g.62943A>T

Select item 122749956.

rs12274995 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:56251694 (GRCh38)
11:56019170 (GRCh37)
Canonical SPDI:: NC_000011.10:56251693:C:A,NC_000011.10:56251693:C:T
Gene:: OR5T3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.006054/183 (ALFA)
T=0.000223/1 (Estonian)
T=0.001002/1 (GoNL)
T=0.003247/1 (HapMap)
T=0.017185/2406 (GnomAD)
T=0.018104/4792 (TOPMED)
T=0.021237/106 (1000Genomes)
T=0.023148/5 (Qatari)
C=0.375/3 (SGDP_PRJ)
HGVS:: NC_000011.10:g.56251694C>A, NC_000011.10:g.56251694C>T, NC_000011.9:g.56019170C>A, NC_000011.9:g.56019170C>T, NW_025791793.1:g.62443C>A, NW_025791793.1:g.62443C>T, NW_003871073.1:g.62443C>A, NW_003871073.1:g.62443C>T

Select item 171502237.

rs17150223 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:56251415 (GRCh38)
11:56018891 (GRCh37)
Canonical SPDI:: NC_000011.10:56251414:G:A
Gene:: OR5T3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.017404/251 (ALFA)
A=0.018519/4 (Qatari)
A=0.022109/3089 (GnomAD)
A=0.02288/6056 (TOPMED)
A=0.026702/134 (1000Genomes)
A=0.033333/11 (HapMap)
G=0.5/7 (SGDP_PRJ)
HGVS:: NC_000011.10:g.56251415G>A, NC_000011.9:g.56018891G>A, NW_025791793.1:g.62164G>A, NW_003871073.1:g.62164G>A

Select item 171502438.

rs17150243 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:56252449 (GRCh38)
11:56019925 (GRCh37)
Canonical SPDI:: NC_000011.10:56252448:T:G
Gene:: OR5T3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.010795/2642 (ALFA)
G=0./0 (PRJEB36033)
G=0.000259/1 (ALSPAC)
G=0.000539/2 (TWINSUK)
G=0.001002/1 (GoNL)
G=0.001667/1 (NorthernSweden)
G=0.001847/24 (GoESP)
G=0.003571/16 (Estonian)
G=0.005618/3 (MGP)
G=0.012397/1737 (GnomAD)
G=0.016447/5 (FINRISK)
G=0.02161/5720 (TOPMED)
G=0.025/1 (GENOME_DK)
G=0.026234/131 (1000Genomes)
G=0.029095/3526 (ExAC)
G=0.034202/21 (Vietnamese)
G=0.035552/8920 (GnomAD_exomes)
G=0.051374/4043 (PAGE_STUDY)
G=0.103675/79 (HapMap)
G=0.143401/113 (PRJEB37584)
G=0.17227/2887 (TOMMO)
G=0.216724/635 (KOREAN)
T=0.5/21 (SGDP_PRJ)
HGVS:: NC_000011.10:g.56252449T>G, NC_000011.9:g.56019925T>G, NW_025791793.1:g.63198T>G, NW_003871073.1:g.63198T>G, NM_001004747.2:c.196T>G, NM_001004747.1:c.250T>G, NP_001004747.2:p.Trp66Gly

Select item 176125659.

rs17612565 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:56252168 (GRCh38)
11:56019644 (GRCh37)
Canonical SPDI:: NC_000011.10:56252167:A:G,NC_000011.10:56252167:A:T
Gene:: OR5T3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.049532/1587 (ALFA)
G=0.036071/181 (1000Genomes)
G=0.045597/58 (HapMap)
G=0.046296/10 (Qatari)
G=0.049503/13103 (TOPMED)
G=0.057319/744 (GoESP)
G=0.057417/8038 (GnomAD)
G=0.064872/12209 (GnomAD_exomes)
G=0.066132/66 (GoNL)
G=0.073731/7181 (ExAC)
G=0.074906/40 (MGP)
G=0.075/3 (GENOME_DK)
G=0.075512/280 (TWINSUK)
G=0.082252/317 (ALSPAC)
G=0.088816/27 (FINRISK)
G=0.095/57 (NorthernSweden)
G=0.101562/455 (Estonian)
A=0.45/18 (SGDP_PRJ)
A=0.5/4 (Siberian)
HGVS:: NC_000011.10:g.56252168A>G, NC_000011.10:g.56252168A>T, NC_000011.9:g.56019644A>G, NC_000011.9:g.56019644A>T, NW_025791793.1:g.62917A>G, NW_025791793.1:g.62917A>T, NW_003871073.1:g.62917A>G, NW_003871073.1:g.62917A>T

Select item 6174655110.

rs61746551 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:56252768 (GRCh38)
11:56020244 (GRCh37)
Canonical SPDI:: NC_000011.10:56252767:T:C
Gene:: OR5T3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.077798/3837 (ALFA)
C=0.000071/2 (TOMMO)
C=0.060119/301 (1000Genomes)
C=0.067134/67 (GoNL)
C=0.068334/17174 (GnomAD_exomes)
C=0.069444/15 (Qatari)
C=0.070739/18724 (TOPMED)
C=0.070768/8590 (ExAC)
C=0.075512/280 (TWINSUK)
C=0.076779/41 (MGP)
C=0.077255/10818 (GnomAD)
C=0.079895/1038 (GoESP)
C=0.082252/317 (ALSPAC)
C=0.095/57 (NorthernSweden)
C=0.101562/455 (Estonian)
T=0.4375/21 (SGDP_PRJ)
HGVS:: NC_000011.10:g.56252768T>C, NC_000011.9:g.56020244T>C, NW_025791793.1:g.63517T>C, NW_003871073.1:g.63517T>C, NM_001004747.2:c.515T>C, NM_001004747.1:c.569T>C, NP_001004747.2:p.Ile172Thr

Select item 6174748011.

rs61747480 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 11:56252962 (GRCh38)
11:56020438 (GRCh37)
Canonical SPDI:: NC_000011.10:56252961:A:C,NC_000011.10:56252961:A:G
Gene:: OR5T3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.001234/252 (ALFA)
C=0.00319/801 (GnomAD_exomes)
C=0.003608/438 (ExAC)
C=0.00463/1 (Qatari)
C=0.011978/1678 (GnomAD)
C=0.012619/3340 (TOPMED)
C=0.013273/66 (1000Genomes)
C=0.014393/187 (GoESP)
C=0.018996/1495 (PAGE_STUDY)
A=0.5/9 (SGDP_PRJ)
HGVS:: NC_000011.10:g.56252962A>C, NC_000011.10:g.56252962A>G, NC_000011.9:g.56020438A>C, NC_000011.9:g.56020438A>G, NW_025791793.1:g.63711A>C, NW_025791793.1:g.63711A>G, NW_003871073.1:g.63711A>C, NW_003871073.1:g.63711A>G, NM_001004747.2:c.709A>C, NM_001004747.2:c.709A>G, NM_001004747.1:c.763A>C, NM_001004747.1:c.763A>G, NP_001004747.2:p.Ile237Leu, NP_001004747.2:p.Ile237Val

Select item 6175091912.

rs61750919 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 11:56253057 (GRCh38)
11:56020533 (GRCh37)
Canonical SPDI:: NC_000011.10:56253056:C:G,NC_000011.10:56253056:C:T
Gene:: OR5T3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.004531/294 (ALFA)
T=0./0 (ALSPAC)
T=0.00027/1 (TWINSUK)
T=0.00481/1207 (GnomAD_exomes)
T=0.00583/707 (ExAC)
T=0.019935/259 (GoESP)
T=0.021814/5774 (TOPMED)
T=0.02436/122 (1000Genomes)
C=0.333333/2 (SGDP_PRJ)
HGVS:: NC_000011.10:g.56253057C>G, NC_000011.10:g.56253057C>T, NC_000011.9:g.56020533C>G, NC_000011.9:g.56020533C>T, NW_025791793.1:g.63806C>G, NW_025791793.1:g.63806C>T, NW_003871073.1:g.63806C>G, NW_003871073.1:g.63806C>T, NM_001004747.2:c.804C>G, NM_001004747.2:c.804C>T, NM_001004747.1:c.858C>G, NM_001004747.1:c.858C>T

Select item 6175341113.

rs61753411 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:56253219 (GRCh38)
11:56020695 (GRCh37)
Canonical SPDI:: NC_000011.10:56253218:A:C
Gene:: OR5T3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.001337/221 (ALFA)
C=0.003752/663 (GnomAD_exomes)
C=0.00463/1 (Qatari)
C=0.005533/360 (ExAC)
C=0.011973/1678 (GnomAD)
C=0.012622/3341 (TOPMED)
C=0.012759/165 (GoESP)
C=0.013273/66 (1000Genomes)
C=0.018996/1495 (PAGE_STUDY)
A=0.5/9 (SGDP_PRJ)
HGVS:: NC_000011.10:g.56253219A>C, NC_000011.9:g.56020695A>C, NW_025791793.1:g.63968A>C, NW_003871073.1:g.63968A>C, NM_001004747.2:c.966A>C, NM_001004747.1:c.1020A>C, NP_001004747.2:p.Lys322Asn

Select item 6188723614.

rs61887236 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:56250768 (GRCh38)
11:56018244 (GRCh37)
Canonical SPDI:: NC_000011.10:56250767:A:G
Gene:: OR5T3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.07369/1392 (ALFA)
G=0.038882/195 (1000Genomes)
G=0.046296/10 (Qatari)
G=0.052552/13910 (TOPMED)
G=0.059963/8373 (GnomAD)
G=0.066132/66 (GoNL)
G=0.075/3 (GENOME_DK)
G=0.075782/281 (TWINSUK)
G=0.082252/317 (ALSPAC)
G=0.095/57 (NorthernSweden)
G=0.101562/455 (Estonian)
A=0.45/18 (SGDP_PRJ)
A=0.5/4 (Siberian)
HGVS:: NC_000011.10:g.56250768A>G, NC_000011.9:g.56018244A>G, NW_025791793.1:g.61517A>G, NW_003871073.1:g.61517A>G

Select item 7347435815.

rs73474358 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:56253139 (GRCh38)
11:56020615 (GRCh37)
Canonical SPDI:: NC_000011.10:56253138:A:G,NC_000011.10:56253138:A:T
Gene:: OR5T3 (Varview)
Functional Consequence:: missense_variant,stop_gained,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000329/68 (ALFA)
G=0.000785/196 (GnomAD_exomes)
G=0.000998/120 (ExAC)
G=0.002812/394 (GnomAD)
G=0.003087/817 (TOPMED)
G=0.003387/44 (GoESP)
G=0.004372/22 (1000Genomes)
G=0.004587/361 (PAGE_STUDY)
HGVS:: NC_000011.10:g.56253139A>G, NC_000011.10:g.56253139A>T, NC_000011.9:g.56020615A>G, NC_000011.9:g.56020615A>T, NW_025791793.1:g.63888A>G, NW_025791793.1:g.63888A>T, NW_003871073.1:g.63888A>G, NW_003871073.1:g.63888A>T, NM_001004747.2:c.886A>G, NM_001004747.2:c.886A>T, NM_001004747.1:c.940A>G, NM_001004747.1:c.940A>T, NP_001004747.2:p.Lys296Glu, NP_001004747.2:p.Lys296Ter

Select item 7480630616.

rs74806306 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:56250399 (GRCh38)
11:56017875 (GRCh37)
Canonical SPDI:: NC_000011.10:56250398:A:C
Gene:: OR5T3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.018377/265 (ALFA)
C=0.009259/2 (Qatari)
C=0.02487/3473 (GnomAD)
C=0.026616/7045 (TOPMED)
C=0.027483/138 (1000Genomes)
A=0.416667/5 (SGDP_PRJ)
HGVS:: NC_000011.10:g.56250399A>C, NC_000011.9:g.56017875A>C, NW_025791793.1:g.61148A>C, NW_003871073.1:g.61148A>C

Select item 7525826617.

rs75258266 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:56251057 (GRCh38)
11:56018533 (GRCh37)
Canonical SPDI:: NC_000011.10:56251056:G:A,NC_000011.10:56251056:G:T
Gene:: OR5T3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.022174/317 (ALFA)
A=0./0 (ALSPAC)
A=0.00027/1 (TWINSUK)
A=0.013889/3 (Qatari)
A=0.035883/5009 (GnomAD)
A=0.038241/10122 (TOPMED)
A=0.040912/205 (1000Genomes)
G=0.444444/8 (SGDP_PRJ)
HGVS:: NC_000011.10:g.56251057G>A, NC_000011.10:g.56251057G>T, NC_000011.9:g.56018533G>A, NC_000011.9:g.56018533G>T, NW_025791793.1:g.61806G>A, NW_025791793.1:g.61806G>T, NW_003871073.1:g.61806G>A, NW_003871073.1:g.61806G>T

Select item 7539475318.

rs75394753 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:56250726 (GRCh38)
11:56018202 (GRCh37)
Canonical SPDI:: NC_000011.10:56250725:A:G
Gene:: OR5T3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.026491/382 (ALFA)
G=0./0 (ALSPAC)
G=0.00027/1 (TWINSUK)
G=0.013889/3 (Qatari)
G=0.035808/5002 (GnomAD)
G=0.038237/10121 (TOPMED)
G=0.040912/205 (1000Genomes)
A=0.444444/8 (SGDP_PRJ)
HGVS:: NC_000011.10:g.56250726A>G, NC_000011.9:g.56018202A>G, NW_025791793.1:g.61475A>G, NW_003871073.1:g.61475A>G

Select item 7571686419.

rs75716864 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:56252573 (GRCh38)
11:56020049 (GRCh37)
Canonical SPDI:: NC_000011.10:56252572:T:C
Gene:: OR5T3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.003662/707 (ALFA)
C=0./0 (TWINSUK)
C=0.000077/1 (GoESP)
C=0.000259/1 (ALSPAC)
C=0.00067/3 (Estonian)
C=0.002091/293 (GnomAD)
C=0.004107/1087 (TOPMED)
C=0.006741/818 (ExAC)
C=0.007208/1811 (GnomAD_exomes)
C=0.01/6 (NorthernSweden)
C=0.015147/76 (1000Genomes)
C=0.018519/4 (Vietnamese)
C=0.086348/253 (KOREAN)
C=0.102166/1712 (TOMMO)
C=0.107595/85 (PRJEB37584)
T=0.5/16 (SGDP_PRJ)
T=0.5/2 (Siberian)
HGVS:: NC_000011.10:g.56252573T>C, NC_000011.9:g.56020049T>C, NW_025791793.1:g.63322T>C, NW_003871073.1:g.63322T>C, NM_001004747.2:c.320T>C, NM_001004747.1:c.374T>C, NP_001004747.2:p.Ile107Thr

Select item 7642714720.

rs76427147 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:56250871 (GRCh38)
11:56018347 (GRCh37)
Canonical SPDI:: NC_000011.10:56250870:A:G
Gene:: OR5T3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000763/11 (ALFA)
G=0.00027/1 (TWINSUK)
G=0.000519/2 (ALSPAC)
G=0.001438/201 (GnomAD)
G=0.00286/757 (TOPMED)
G=0.011868/59 (1000Genomes)
G=0.042056/9 (Vietnamese)
G=0.054466/913 (TOMMO)
G=0.066212/194 (KOREAN)
A=0.5/10 (SGDP_PRJ)
A=0.5/2 (Siberian)
HGVS:: NC_000011.10:g.56250871A>G, NC_000011.9:g.56018347A>G, NW_025791793.1:g.61620A>G, NW_003871073.1:g.61620A>G

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