OR52M1 - SNP

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Select item 15052111.

rs1505211 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:4543640 (GRCh38)
11:4564870 (GRCh37)
Canonical SPDI:: NC_000011.10:4543639:G:A,NC_000011.10:4543639:G:C
Gene:: OR52M1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.002591/36 (ALFA)
A=0.002004/2 (GoNL)
A=0.002595/10 (ALSPAC)
A=0.002967/11 (TWINSUK)
A=0.045732/15 (HapMap)
A=0.050399/13340 (TOPMED)
A=0.051999/260 (1000Genomes)
A=0.055556/12 (Qatari)
G=0.375/9 (SGDP_PRJ)
HGVS:: NC_000011.10:g.4543640G>A, NC_000011.10:g.4543640G>C, NC_000011.9:g.4564870G>A, NC_000011.9:g.4564870G>C

Select item 15052122.

rs1505212 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 11:4543468 (GRCh38)
11:4564698 (GRCh37)
Canonical SPDI:: NC_000011.10:4543467:C:A,NC_000011.10:4543467:C:G
Gene:: OR52M1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.002271/31 (ALFA)
G=0.002004/2 (GoNL)
G=0.002854/11 (ALSPAC)
G=0.003506/13 (TWINSUK)
G=0.042945/14 (HapMap)
G=0.045427/6365 (GnomAD)
G=0.046813/12391 (TOPMED)
G=0.047314/237 (1000Genomes)
G=0.060185/13 (Qatari)
C=0.423077/11 (SGDP_PRJ)
HGVS:: NC_000011.10:g.4543468C>A, NC_000011.10:g.4543468C>G, NC_000011.9:g.4564698C>A, NC_000011.9:g.4564698C>G

Select item 25662703.

rs2566270 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:4544200 (GRCh38)
11:4565430 (GRCh37)
Canonical SPDI:: NC_000011.10:4544199:A:G,NC_000011.10:4544199:A:T
Gene:: OR52M1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.49526/8881 (ALFA)
G=0.309524/65 (Vietnamese)
A=0.332418/121 (SGDP_PRJ)
G=0.33955/5690 (TOMMO)
G=0.362799/1063 (KOREAN)
A=0.4/16 (Siberian)
A=0.425/17 (GENOME_DK)
G=0.458333/275 (NorthernSweden)
A=0.479611/67134 (GnomAD)
A=0.481481/104 (Qatari)
A=0.481661/1786 (TWINSUK)
G=0.482118/2413 (1000Genomes)
A=0.487468/129028 (TOPMED)
A=0.488324/1882 (ALSPAC)
G=0.491964/2204 (Estonian)
G=0.491984/491 (GoNL)
HGVS:: NC_000011.10:g.4544200A>G, NC_000011.10:g.4544200A>T, NC_000011.9:g.4565430A>G, NC_000011.9:g.4565430A>T

Select item 26414124.

rs2641412 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:4544260 (GRCh38)
11:4565490 (GRCh37)
Canonical SPDI:: NC_000011.10:4544259:G:A,NC_000011.10:4544259:G:T
Gene:: OR52M1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.486767/25601 (ALFA)
G=0.332418/121 (SGDP_PRJ)
A=0.339408/5688 (TOMMO)
A=0.362116/1061 (KOREAN)
G=0.4/16 (Siberian)
G=0.425/17 (GENOME_DK)
A=0.458333/275 (NorthernSweden)
A=0.464012/967 (HGDP_Stanford)
G=0.481661/1786 (TWINSUK)
A=0.483916/2423 (1000Genomes)
G=0.486111/105 (Qatari)
G=0.486584/128794 (TOPMED)
G=0.488583/1883 (ALSPAC)
A=0.489955/2195 (Estonian)
A=0.491984/491 (GoNL)
G=0.5/946 (HapMap)
HGVS:: NC_000011.10:g.4544260G>A, NC_000011.10:g.4544260G>T, NC_000011.9:g.4565490G>A, NC_000011.9:g.4565490G>T

Select item 26571675.

rs2657167 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 11:4546105 (GRCh38)
11:4567335 (GRCh37)
Canonical SPDI:: NC_000011.10:4546104:C:A,NC_000011.10:4546104:C:G
Gene:: OR52M1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.407072/21193 (ALFA)
G=0.137143/72 (Vietnamese)
G=0.312734/167 (MGP)
G=0.317073/26 (PRJEB36033)
G=0.34001/5698 (TOMMO)
G=0.355263/108 (FINRISK)
G=0.356667/214 (NorthernSweden)
G=0.362799/1063 (KOREAN)
G=0.368527/1651 (Estonian)
G=0.370513/289 (PRJEB37584)
C=0.375758/124 (SGDP_PRJ)
G=0.390782/390 (GoNL)
G=0.392665/1456 (TWINSUK)
G=0.393358/1516 (ALSPAC)
C=0.394737/15 (Siberian)
G=0.419528/33016 (PAGE_STUDY)
G=0.421296/91 (Qatari)
G=0.424172/112274 (TOPMED)
G=0.425671/2132 (1000Genomes)
G=0.429595/60109 (GnomAD)
G=0.430233/814 (HapMap)
G=0.444299/5775 (GoESP)
G=0.45/18 (GENOME_DK)
HGVS:: NC_000011.10:g.4546105C>A, NC_000011.10:g.4546105C>G, NC_000011.9:g.4567335C>A, NC_000011.9:g.4567335C>G, NM_001004137.1:c.915C>A, NM_001004137.1:c.915C>G, NP_001004137.1:p.Ser305Arg, NP_001004137.1:p.Ser305Arg

Select item 26571686.

rs2657168 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:4545147 (GRCh38)
11:4566377 (GRCh37)
Canonical SPDI:: NC_000011.10:4545146:C:T
Gene:: OR52M1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.37306/108112 (ALFA)
T=0.149813/80 (MGP)
T=0.226852/49 (Vietnamese)
T=0.290525/22862 (PAGE_STUDY)
T=0.308184/241 (PRJEB37584)
T=0.31085/5209 (TOMMO)
T=0.312969/917 (KOREAN)
T=0.319869/586 (Korea1K)
T=0.324339/613 (HapMap)
T=0.324641/1626 (1000Genomes)
T=0.327255/682 (HGDP_Stanford)
C=0.333333/2 (PRJEB36033)
T=0.336667/202 (NorthernSweden)
T=0.336752/89135 (TOPMED)
T=0.34109/58089 (GnomAD_exomes)
T=0.343267/48019 (GnomAD)
T=0.343304/1538 (Estonian)
T=0.345283/36763 (ExAC)
T=0.355747/4624 (GoESP)
T=0.363727/363 (GoNL)
T=0.37037/80 (Qatari)
C=0.370504/103 (SGDP_PRJ)
T=0.383498/1478 (ALSPAC)
T=0.384574/1426 (TWINSUK)
C=0.411765/14 (Siberian)
T=0.45/18 (GENOME_DK)
HGVS:: NC_000011.10:g.4545147C>T, NC_000011.9:g.4566377C>T

Select item 27091827.

rs2709182 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 11:4545481 (GRCh38)
11:4566711 (GRCh37)
Canonical SPDI:: NC_000011.10:4545480:C:A,NC_000011.10:4545480:C:G,NC_000011.10:4545480:C:T
Gene:: OR52M1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.491656/72828 (ALFA)
T=0.25/54 (Vietnamese)
T=0.310602/5205 (TOMMO)
T=0.311134/911 (KOREAN)
T=0.320415/587 (Korea1K)
C=0.356287/119 (SGDP_PRJ)
T=0.404605/123 (FINRISK)
C=0.421053/16 (Siberian)
A=0.42151/33172 (PAGE_STUDY)
C=0.425/17 (GENOME_DK)
T=0.43832/2195 (1000Genomes)
T=0.441737/834 (HapMap)
T=0.456667/274 (NorthernSweden)
C=0.477528/255 (MGP)
T=0.47845/126641 (TOPMED)
C=0.48274/1790 (TWINSUK)
T=0.486111/105 (Qatari)
C=0.486306/6321 (GoESP)
C=0.489621/1887 (ALSPAC)
T=0.490982/490 (GoNL)
T=0.491518/2202 (Estonian)
C=0.499117/565 (Daghestan)
HGVS:: NC_000011.10:g.4545481C>A, NC_000011.10:g.4545481C>G, NC_000011.10:g.4545481C>T, NC_000011.9:g.4566711C>A, NC_000011.9:g.4566711C>G, NC_000011.9:g.4566711C>T, NM_001004137.1:c.291C>A, NM_001004137.1:c.291C>G, NM_001004137.1:c.291C>T, NP_001004137.1:p.Asp97Glu, NP_001004137.1:p.Asp97Glu

Select item 27091858.

rs2709185 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:4543432 (GRCh38)
11:4564662 (GRCh37)
Canonical SPDI:: NC_000011.10:4543431:C:A,NC_000011.10:4543431:C:T
Gene:: OR52M1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.391008/5392 (ALFA)
T=0.303738/65 (Vietnamese)
T=0.339019/5681 (TOMMO)
C=0.358824/122 (SGDP_PRJ)
T=0.362457/1062 (KOREAN)
C=0.4/16 (Siberian)
C=0.425/17 (GENOME_DK)
T=0.432432/32 (PRJEB36033)
T=0.434416/2176 (1000Genomes)
T=0.449074/97 (Qatari)
T=0.458333/275 (NorthernSweden)
T=0.465658/123255 (TOPMED)
T=0.475425/66473 (GnomAD)
T=0.47546/155 (HapMap)
C=0.484088/1795 (TWINSUK)
T=0.48998/489 (GoNL)
C=0.490659/1891 (ALSPAC)
T=0.491518/2202 (Estonian)
HGVS:: NC_000011.10:g.4543432C>A, NC_000011.10:g.4543432C>T, NC_000011.9:g.4564662C>A, NC_000011.9:g.4564662C>T

Select item 65784999.

rs6578499 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:4544584 (GRCh38)
11:4565814 (GRCh37)
Canonical SPDI:: NC_000011.10:4544583:G:A,NC_000011.10:4544583:G:T
Gene:: OR52M1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.004721/1069 (ALFA)
T=0.000071/2 (TOMMO)
A=0.001002/1 (GoNL)
A=0.018519/4 (Qatari)
A=0.044747/11844 (TOPMED)
A=0.049656/249 (1000Genomes)
A=0.065235/5134 (PAGE_STUDY)
A=0.081818/90 (HapMap)
G=0.5/8 (SGDP_PRJ)
HGVS:: NC_000011.10:g.4544584G>A, NC_000011.10:g.4544584G>T, NC_000011.9:g.4565814G>A, NC_000011.9:g.4565814G>T

Select item 710168810.

rs7101688 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:4546354 (GRCh38)
11:4567584 (GRCh37)
Canonical SPDI:: NC_000011.10:4546353:A:G
Gene:: OR52M1 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.412709/7839 (ALFA)
G=0.240741/52 (Vietnamese)
G=0.31131/5217 (TOMMO)
G=0.312287/915 (KOREAN)
G=0.320961/588 (Korea1K)
G=0.368333/221 (NorthernSweden)
A=0.377483/114 (SGDP_PRJ)
G=0.392879/1968 (1000Genomes)
G=0.402455/1803 (Estonian)
G=0.402778/87 (Qatari)
G=0.403192/106721 (TOPMED)
G=0.403808/403 (GoNL)
G=0.406688/1508 (TWINSUK)
G=0.408926/1576 (ALSPAC)
G=0.412652/57763 (GnomAD)
A=0.416667/15 (Siberian)
G=0.435739/495 (Daghestan)
G=0.451515/149 (HapMap)
G=0.475/19 (GENOME_DK)
HGVS:: NC_000011.10:g.4546354A>G, NC_000011.9:g.4567584A>G

Select item 711201011.

rs7112010 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:4545216 (GRCh38)
11:4566446 (GRCh37)
Canonical SPDI:: NC_000011.10:4545215:C:T
Gene:: OR52M1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000645/131 (ALFA)
T=0.001341/328 (GnomAD_exomes)
T=0.00177/203 (ExAC)
T=0.00463/1 (Qatari)
T=0.005248/1389 (TOPMED)
T=0.005539/72 (GoESP)
T=0.005683/796 (GnomAD)
T=0.008768/690 (PAGE_STUDY)
T=0.008901/45 (1000Genomes)
T=0.014512/22 (HapMap)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000011.10:g.4545216C>T, NC_000011.9:g.4566446C>T, NM_001004137.1:c.26C>T, NP_001004137.1:p.Ser9Leu

Select item 1055775412.

rs10557754 [Homo sapiens]

Variant type:: DELINS
Alleles:: GCT>-,GCTGCT [Show Flanks]
Chromosome:: 11:4546390 (GRCh38)
11:4567620 (GRCh37)
Canonical SPDI:: NC_000011.10:4546386:GCTGCT:GCT,NC_000011.10:4546386:GCTGCT:GCTGCTGCT
Gene:: OR52M1 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GCTGCT=0.426674/7902 (ALFA)
-=0.310185/67 (Vietnamese)
-=0.339975/5697 (TOMMO)
-=0.368333/221 (NorthernSweden)
-=0.401786/1800 (Estonian)
-=0.407767/1512 (TWINSUK)
-=0.407816/407 (GoNL)
-=0.409704/1579 (ALSPAC)
-=0.428795/2147 (1000Genomes)
-=0.433322/114696 (TOPMED)
-=0.439556/61428 (GnomAD)
-=0.475/19 (GENOME_DK)
HGVS:: NC_000011.10:g.4546387GCT[1], NC_000011.10:g.4546387GCT[3], NC_000011.9:g.4567617GCT[1], NC_000011.9:g.4567617GCT[3]

Select item 1083625413.

rs10836254 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:4546615 (GRCh38)
11:4567845 (GRCh37)
Canonical SPDI:: NC_000011.10:4546614:T:A,NC_000011.10:4546614:T:C
Gene:: OR52M1 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.422393/7979 (ALFA)
A=0.116232/116 (GoNL)
A=0.300926/65 (Vietnamese)
A=0.339161/5684 (TOMMO)
A=0.361433/1059 (KOREAN)
A=0.368333/221 (NorthernSweden)
T=0.376543/122 (SGDP_PRJ)
A=0.384259/83 (Qatari)
T=0.394737/15 (Siberian)
A=0.402455/1803 (Estonian)
A=0.405879/1505 (TWINSUK)
A=0.407888/1572 (ALSPAC)
A=0.419928/2103 (1000Genomes)
A=0.422441/111816 (TOPMED)
A=0.431053/60313 (GnomAD)
A=0.475/19 (GENOME_DK)
A=0.477848/151 (HapMap)
HGVS:: NC_000011.10:g.4546615T>A, NC_000011.10:g.4546615T>C, NC_000011.9:g.4567845T>A, NC_000011.9:g.4567845T>C

Select item 1103273814.

rs11032738 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 11:4545283 (GRCh38)
11:4566513 (GRCh37)
Canonical SPDI:: NC_000011.10:4545282:C:A,NC_000011.10:4545282:C:G
Gene:: OR52M1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.006821/338 (ALFA)
A=0.001093/5 (1000Genomes)
A=0.001873/1 (MGP)
A=0.003289/1 (FINRISK)
A=0.004018/18 (Estonian)
A=0.004568/1209 (TOPMED)
A=0.00501/5 (GoNL)
A=0.005206/730 (GnomAD)
A=0.006667/4 (NorthernSweden)
A=0.007001/91 (GoESP)
A=0.007525/29 (ALSPAC)
A=0.010518/39 (TWINSUK)
A=0.025/1 (GENOME_DK)
C=0.5/1 (SGDP_PRJ)
C=0.5/1 (Siberian)
HGVS:: NC_000011.10:g.4545283C>A, NC_000011.10:g.4545283C>G, NC_000011.9:g.4566513C>A, NC_000011.9:g.4566513C>G, NM_001004137.1:c.93C>A, NM_001004137.1:c.93C>G, NP_001004137.1:p.Ile31Met

Select item 1140006015.

rs11400060 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 11:4546522 (GRCh38)
11:4567753 (GRCh37)
Canonical SPDI:: NC_000011.10:4546522:T:TT
Gene:: OR52M1 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0.410745/7607 (ALFA)
T=0.238318/51 (Vietnamese)
T=0.311239/5216 (TOMMO)
T=0.320415/587 (Korea1K)
T=0.368333/221 (NorthernSweden)
T=0.392723/1967 (1000Genomes)
T=0.401116/1797 (Estonian)
T=0.402101/106432 (TOPMED)
T=0.403808/403 (GoNL)
T=0.410489/57319 (GnomAD)
T=0.475/19 (GENOME_DK)
HGVS:: NC_000011.10:g.4546523dup, NC_000011.9:g.4567753dup

Select item 1228042416.

rs12280424 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:4544297 (GRCh38)
11:4565527 (GRCh37)
Canonical SPDI:: NC_000011.10:4544296:G:A
Gene:: OR52M1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.11376/16646 (ALFA)
A=0.028664/480 (TOMMO)
A=0.049829/146 (KOREAN)
A=0.096845/485 (1000Genomes)
A=0.101667/61 (NorthernSweden)
A=0.10521/105 (GoNL)
A=0.106481/23 (Qatari)
A=0.108803/28799 (TOPMED)
A=0.114601/15406 (GnomAD)
A=0.120135/463 (ALSPAC)
A=0.122823/550 (Estonian)
A=0.125/5 (GENOME_DK)
A=0.126455/239 (HapMap)
A=0.127023/471 (TWINSUK)
G=0.44898/44 (SGDP_PRJ)
G=0.5/3 (Siberian)
HGVS:: NC_000011.10:g.4544297G>A, NC_000011.9:g.4565527G>A

Select item 1228052217.

rs12280522 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 11:4544433 (GRCh38)
11:4565663 (GRCh37)
Canonical SPDI:: NC_000011.10:4544432:G:C,NC_000011.10:4544432:G:T
Gene:: OR52M1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.039852/688 (ALFA)
C=0.033333/11 (HapMap)
C=0.03857/193 (1000Genomes)
C=0.068272/18071 (TOPMED)
C=0.068748/9634 (GnomAD)
C=0.083333/18 (Qatari)
C=0.086172/86 (GoNL)
C=0.089286/400 (Estonian)
C=0.09/54 (NorthernSweden)
C=0.100934/389 (ALSPAC)
C=0.110572/410 (TWINSUK)
G=0.447368/17 (SGDP_PRJ)
G=0.5/1 (Siberian)
HGVS:: NC_000011.10:g.4544433G>C, NC_000011.10:g.4544433G>T, NC_000011.9:g.4565663G>C, NC_000011.9:g.4565663G>T

Select item 1229260518.

rs12292605 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:4544975 (GRCh38)
11:4566205 (GRCh37)
Canonical SPDI:: NC_000011.10:4544974:A:G
Gene:: OR52M1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.113896/2849 (ALFA)
G=0.046065/231 (1000Genomes)
G=0.073113/93 (HapMap)
G=0.083494/22100 (TOPMED)
G=0.088538/12416 (GnomAD)
G=0.092593/20 (Qatari)
G=0.121667/73 (NorthernSweden)
G=0.123246/123 (GoNL)
G=0.125/5 (GENOME_DK)
G=0.126362/487 (ALSPAC)
G=0.131877/489 (TWINSUK)
G=0.147991/663 (Estonian)
A=0.431818/19 (SGDP_PRJ)
A=0.5/2 (Siberian)
HGVS:: NC_000011.10:g.4544975A>G, NC_000011.9:g.4566205A>G

Select item 1229589819.

rs12295898 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:4545955 (GRCh38)
11:4567185 (GRCh37)
Canonical SPDI:: NC_000011.10:4545954:T:A,NC_000011.10:4545954:T:C
Gene:: OR52M1 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.099632/17543 (ALFA)
C=0.038101/191 (1000Genomes)
C=0.039474/12 (FINRISK)
C=0.06338/72 (Daghestan)
C=0.063679/81 (HapMap)
C=0.066274/17542 (TOPMED)
C=0.067085/9403 (GnomAD)
C=0.069733/8459 (ExAC)
C=0.075319/979 (GoESP)
C=0.083333/18 (Qatari)
C=0.086172/86 (GoNL)
C=0.088839/398 (Estonian)
C=0.09/54 (NorthernSweden)
C=0.098858/381 (ALSPAC)
C=0.1/4 (GENOME_DK)
C=0.109223/405 (TWINSUK)
C=0.110487/59 (MGP)
T=0.447368/17 (SGDP_PRJ)
T=0.5/1 (Siberian)
HGVS:: NC_000011.10:g.4545955T>A, NC_000011.10:g.4545955T>C, NC_000011.9:g.4567185T>A, NC_000011.9:g.4567185T>C, NM_001004137.1:c.765T>A, NM_001004137.1:c.765T>C, NP_001004137.1:p.Tyr255Ter

Select item 1691135620.

rs16911356 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:4546528 (GRCh38)
11:4567758 (GRCh37)
Canonical SPDI:: NC_000011.10:4546527:A:G,NC_000011.10:4546527:A:T
Gene:: OR52M1 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.40062/7232 (ALFA)
G=0.236111/51 (Vietnamese)
G=0.311239/5216 (TOMMO)
G=0.311945/914 (KOREAN)
G=0.320415/587 (Korea1K)
G=0.368333/221 (NorthernSweden)
A=0.376667/113 (SGDP_PRJ)
G=0.392723/1967 (1000Genomes)
G=0.401116/1797 (Estonian)
G=0.402778/87 (Qatari)
G=0.402932/106652 (TOPMED)
G=0.403808/403 (GoNL)
G=0.406958/1509 (TWINSUK)
G=0.407369/1570 (ALSPAC)
G=0.410667/57357 (GnomAD)
A=0.416667/15 (Siberian)
G=0.475/19 (GENOME_DK)
HGVS:: NC_000011.10:g.4546528A>G, NC_000011.10:g.4546528A>T, NC_000011.9:g.4567758A>G, NC_000011.9:g.4567758A>T

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