TRIM24 - SNP

Search results

Items: 1 to 20 of 49495

<< First< Prev

Page of 2475

Next >Last >>

Select item 617519671.

rs61751967 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 7:138580592 (GRCh38)
7:138265337 (GRCh37)
Canonical SPDI:: NC_000007.14:138580591:C:G
Gene:: TRIM24 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.008975/1028 (ALFA)
G=0.00203/10 (1000Genomes)
G=0.002694/212 (PAGE_STUDY)
G=0.005625/1489 (TOPMED)
G=0.006535/916 (GnomAD)
G=0.006579/2 (FINRISK)
G=0.007491/4 (MGP)
G=0.007579/1902 (GnomAD_exomes)
G=0.008282/1005 (ExAC)
G=0.008688/113 (GoESP)
G=0.008822/34 (ALSPAC)
G=0.009709/36 (TWINSUK)
G=0.012024/12 (GoNL)
G=0.014509/65 (Estonian)
G=0.025/1 (GENOME_DK)
G=0.043333/26 (NorthernSweden)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000007.14:g.138580592C>G, NC_000007.13:g.138265337C>G, NG_023286.1:g.125259C>G, NM_003852.4:c.2514C>G, NM_003852.3:c.2514C>G, NM_015905.3:c.2616C>G, NM_015905.2:c.2616C>G, XM_024446981.2:c.2559C>G, XM_024446981.1:c.2559C>G, NP_003843.3:p.Asp838Glu, NP_056989.2:p.Asp872Glu, XP_024302749.1:p.Asp853Glu

Select item 129062.

rs12906 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:138585228 (GRCh38)
7:138269973 (GRCh37)
Canonical SPDI:: NC_000007.14:138585227:A:C
Gene:: TRIM24 (Varview)
Functional Consequence:: 3_prime_UTR_variant
HGVS:: NC_000007.14:g.138585228A>C, NC_000007.13:g.138269973A>C, NG_023286.1:g.129895A>C, NM_003852.4:c.*277A>C, NM_003852.3:c.*277A>C, NM_015905.3:c.*277A>C, NM_015905.2:c.*277A>C, XM_024446981.2:c.*277A>C, XM_024446981.1:c.*277A>C

Select item 7280923.

rs728092 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 7:138573916 (GRCh38)
7:138258661 (GRCh37)
Canonical SPDI:: NC_000007.14:138573915:A:C,NC_000007.14:138573915:A:G,NC_000007.14:138573915:A:T
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.135526/1809 (ALFA)
C=0.194444/42 (Qatari)
C=0.228333/137 (NorthernSweden)
C=0.25/10 (GENOME_DK)
C=0.265531/265 (GoNL)
C=0.268527/1203 (Estonian)
C=0.268907/71177 (TOPMED)
C=0.314179/1573 (1000Genomes)
A=0.357143/5 (Siberian)
A=0.359756/118 (SGDP_PRJ)
C=0.425234/91 (Vietnamese)
A=0.427206/7159 (TOMMO)
A=0.478498/1402 (KOREAN)
A=0.480895/881 (Korea1K)
HGVS:: NC_000007.14:g.138573916A>C, NC_000007.14:g.138573916A>G, NC_000007.14:g.138573916A>T, NC_000007.13:g.138258661A>C, NC_000007.13:g.138258661A>G, NC_000007.13:g.138258661A>T, NG_023286.1:g.118583A>C, NG_023286.1:g.118583A>G, NG_023286.1:g.118583A>T

Select item 7495464.

rs749546 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 7:138472334 (GRCh38)
7:138157079 (GRCh37)
Canonical SPDI:: NC_000007.14:138472333:G:A,NC_000007.14:138472333:G:C
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.294261/73829 (ALFA)
A=0.171296/37 (Qatari)
A=0.244974/463 (HapMap)
A=0.264824/37033 (GnomAD)
A=0.266323/70493 (TOPMED)
A=0.273427/21516 (PAGE_STUDY)
A=0.28/168 (NorthernSweden)
A=0.280294/1404 (1000Genomes)
A=0.296316/1142 (ALSPAC)
A=0.300701/1115 (TWINSUK)
A=0.311623/311 (GoNL)
A=0.321652/1441 (Estonian)
G=0.363014/106 (SGDP_PRJ)
A=0.375/15 (GENOME_DK)
G=0.4/8 (Siberian)
A=0.420128/263 (Chileans)
G=0.445978/7474 (TOMMO)
G=0.463198/365 (PRJEB37584)
G=0.48417/887 (Korea1K)
G=0.488737/1432 (KOREAN)
HGVS:: NC_000007.14:g.138472334G>A, NC_000007.14:g.138472334G>C, NC_000007.13:g.138157079G>A, NC_000007.13:g.138157079G>C, NG_023286.1:g.17001G>A, NG_023286.1:g.17001G>C

Select item 8886095.

rs888609 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 7:138472214 (GRCh38)
7:138156959 (GRCh37)
Canonical SPDI:: NC_000007.14:138472213:A:G,NC_000007.14:138472213:A:T
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.16417/2214 (ALFA)
G=0.175926/38 (Qatari)
G=0.266538/70550 (TOPMED)
G=0.275/165 (NorthernSweden)
G=0.280762/1406 (1000Genomes)
G=0.296575/1143 (ALSPAC)
G=0.300701/1115 (TWINSUK)
G=0.311623/311 (GoNL)
G=0.320982/1438 (Estonian)
A=0.363014/106 (SGDP_PRJ)
G=0.375/15 (GENOME_DK)
A=0.4/8 (Siberian)
A=0.446549/7483 (TOMMO)
A=0.48417/887 (Korea1K)
A=0.488396/1431 (KOREAN)
HGVS:: NC_000007.14:g.138472214A>G, NC_000007.14:g.138472214A>T, NC_000007.13:g.138156959A>G, NC_000007.13:g.138156959A>T, NG_023286.1:g.16881A>G, NG_023286.1:g.16881A>T

Select item 9035806.

rs903580 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:138469562 (GRCh38)
7:138154307 (GRCh37)
Canonical SPDI:: NC_000007.14:138469561:A:G
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.001059/20 (ALFA)
G=0.000223/1 (Estonian)
G=0.001712/240 (GnomAD)
G=0.001927/510 (TOPMED)
G=0.002186/11 (1000Genomes)
HGVS:: NC_000007.14:g.138469562A>G, NC_000007.13:g.138154307A>G, NG_023286.1:g.14229A>G

Select item 9852997.

rs985299 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:138527056 (GRCh38)
7:138211801 (GRCh37)
Canonical SPDI:: NC_000007.14:138527055:T:C
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.197041/3743 (ALFA)
T=0.125/5 (Siberian)
T=0.160321/160 (GoNL)
T=0.16684/643 (ALSPAC)
T=0.174757/648 (TWINSUK)
T=0.175/105 (NorthernSweden)
T=0.187012/26163 (GnomAD)
T=0.193664/51261 (TOPMED)
T=0.194444/42 (Qatari)
T=0.208163/102 (SGDP_PRJ)
T=0.214724/70 (HapMap)
T=0.242504/275 (Daghestan)
T=0.25/10 (GENOME_DK)
T=0.260937/1169 (Estonian)
T=0.267801/1341 (1000Genomes)
T=0.416838/6985 (TOMMO)
C=0.453271/97 (Vietnamese)
T=0.46314/1357 (KOREAN)
T=0.467249/856 (Korea1K)
HGVS:: NC_000007.14:g.138527056T>C, NC_000007.13:g.138211801T>C, NG_023286.1:g.71723T>C

Select item 10309618.

rs1030961 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 7:138522830 (GRCh38)
7:138207575 (GRCh37)
Canonical SPDI:: NC_000007.14:138522829:A:C,NC_000007.14:138522829:A:G
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.199576/3770 (ALFA)
A=0.125/5 (Siberian)
A=0.165331/165 (GoNL)
A=0.169953/655 (ALSPAC)
A=0.175/105 (NorthernSweden)
A=0.179612/666 (TWINSUK)
A=0.194196/27203 (GnomAD)
A=0.20102/53208 (TOPMED)
A=0.203704/44 (Qatari)
A=0.206967/101 (SGDP_PRJ)
A=0.208333/25 (HapMap)
A=0.25625/1148 (Estonian)
A=0.275/11 (GENOME_DK)
A=0.275609/1380 (1000Genomes)
A=0.41659/6981 (TOMMO)
A=0.462116/1354 (KOREAN)
A=0.466703/855 (Korea1K)
G=0.476636/102 (Vietnamese)
HGVS:: NC_000007.14:g.138522830A>C, NC_000007.14:g.138522830A>G, NC_000007.13:g.138207575A>C, NC_000007.13:g.138207575A>G, NG_023286.1:g.67497A>C, NG_023286.1:g.67497A>G

Select item 10601549.

rs1060154 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:138577540 (GRCh38)
7:138262285 (GRCh37)
Canonical SPDI:: NC_000007.14:138577539:T:A
Gene:: TRIM24 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000007.14:g.138577540T>A, NC_000007.13:g.138262285T>A, NG_023286.1:g.122207T>A, NM_003852.4:c.2106T>A, NM_003852.3:c.2106T>A, NM_015905.3:c.2208T>A, NM_015905.2:c.2208T>A, XM_024446981.2:c.2151T>A, XM_024446981.1:c.2151T>A

Select item 107325410.

rs1073254 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 7:138546637 (GRCh38)
7:138231382 (GRCh37)
Canonical SPDI:: NC_000007.14:138546636:G:A,NC_000007.14:138546636:G:T
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00167/43 (ALFA)
A=0./0 (HapMap)
A=0.004673/655 (GnomAD)
A=0.005146/1362 (TOPMED)
A=0.005934/30 (1000Genomes)
HGVS:: NC_000007.14:g.138546637G>A, NC_000007.14:g.138546637G>T, NC_000007.13:g.138231382G>A, NC_000007.13:g.138231382G>T, NG_023286.1:g.91304G>A, NG_023286.1:g.91304G>T

Select item 107325511.

rs1073255 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:138546856 (GRCh38)
7:138231601 (GRCh37)
Canonical SPDI:: NC_000007.14:138546855:C:T
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.013245/191 (ALFA)
T=0.00027/1 (TWINSUK)
T=0.000519/2 (ALSPAC)
T=0.001002/1 (GoNL)
T=0.013889/3 (Qatari)
T=0.019636/2752 (GnomAD)
T=0.021746/5756 (TOPMED)
T=0.023026/7 (HapMap)
T=0.024984/125 (1000Genomes)
C=0.5/5 (SGDP_PRJ)
HGVS:: NC_000007.14:g.138546856C>T, NC_000007.13:g.138231601C>T, NG_023286.1:g.91523C>T

Select item 107777212.

rs1077772 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 7:138467686 (GRCh38)
7:138152431 (GRCh37)
Canonical SPDI:: NC_000007.14:138467685:G:C,NC_000007.14:138467685:G:T
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.162811/5490 (ALFA)
G=0.111111/24 (Qatari)
G=0.130261/130 (GoNL)
G=0.139336/537 (ALSPAC)
G=0.14644/543 (TWINSUK)
G=0.156667/94 (NorthernSweden)
G=0.165993/23260 (GnomAD)
G=0.166667/7 (Siberian)
G=0.171457/45383 (TOPMED)
G=0.197959/97 (SGDP_PRJ)
G=0.225/9 (GENOME_DK)
G=0.235729/446 (HapMap)
G=0.237277/1063 (Estonian)
G=0.254841/1276 (1000Genomes)
G=0.416271/6976 (TOMMO)
T=0.45283/96 (Vietnamese)
G=0.462799/1356 (KOREAN)
G=0.465066/852 (Korea1K)
HGVS:: NC_000007.14:g.138467686G>C, NC_000007.14:g.138467686G>T, NC_000007.13:g.138152431G>C, NC_000007.13:g.138152431G>T, NG_023286.1:g.12353G>C, NG_023286.1:g.12353G>T

Select item 136305313.

rs1363053 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:138550898 (GRCh38)
7:138235643 (GRCh37)
Canonical SPDI:: NC_000007.14:138550897:G:C
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.210482/3976 (ALFA)
G=0.157895/6 (Siberian)
G=0.158385/51 (HapMap)
G=0.170403/45104 (TOPMED)
G=0.171296/37 (Qatari)
G=0.17185/24081 (GnomAD)
G=0.176587/89 (SGDP_PRJ)
G=0.200401/200 (GoNL)
G=0.201868/778 (ALSPAC)
G=0.208738/774 (TWINSUK)
G=0.219082/1097 (1000Genomes)
G=0.225/135 (NorthernSweden)
G=0.3125/1400 (Estonian)
G=0.35/14 (GENOME_DK)
G=0.393942/6602 (TOMMO)
G=0.422526/1238 (KOREAN)
G=0.431769/791 (Korea1K)
G=0.462264/98 (Vietnamese)
HGVS:: NC_000007.14:g.138550898G>C, NC_000007.13:g.138235643G>C, NG_023286.1:g.95565G>C

Select item 142160414.

rs1421604 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:138491793 (GRCh38)
7:138176538 (GRCh37)
Canonical SPDI:: NC_000007.14:138491792:C:G,NC_000007.14:138491792:C:T
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.204341/4896 (ALFA)
C=0.15/6 (Siberian)
C=0.165331/165 (GoNL)
C=0.172029/663 (ALSPAC)
C=0.175/105 (NorthernSweden)
C=0.180151/668 (TWINSUK)
C=0.18721/26218 (GnomAD)
C=0.19349/51215 (TOPMED)
C=0.194444/42 (Qatari)
C=0.209016/102 (SGDP_PRJ)
C=0.248943/471 (HapMap)
C=0.2625/1176 (Estonian)
C=0.263585/1320 (1000Genomes)
C=0.275/11 (GENOME_DK)
C=0.417333/6994 (TOMMO)
C=0.462799/1356 (KOREAN)
C=0.463974/850 (Korea1K)
T=0.485849/103 (Vietnamese)
HGVS:: NC_000007.14:g.138491793C>G, NC_000007.14:g.138491793C>T, NC_000007.13:g.138176538C>G, NC_000007.13:g.138176538C>T, NG_023286.1:g.36460C>G, NG_023286.1:g.36460C>T

Select item 153013415.

rs1530134 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:138572462 (GRCh38)
7:138257207 (GRCh37)
Canonical SPDI:: NC_000007.14:138572461:A:G
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0./0 (SGDP_PRJ)
HGVS:: NC_000007.14:g.138572462A>G, NC_000007.13:g.138257207A>G, NG_023286.1:g.117129A>G

Select item 154473316.

rs1544733 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 7:138546075 (GRCh38)
7:138230820 (GRCh37)
Canonical SPDI:: NC_000007.14:138546074:C:A,NC_000007.14:138546074:C:T
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.201307/13035 (ALFA)
C=0.125/5 (Siberian)
C=0.166333/166 (GoNL)
C=0.171251/660 (ALSPAC)
C=0.175/105 (NorthernSweden)
C=0.179881/667 (TWINSUK)
C=0.179999/25211 (GnomAD)
C=0.185919/49211 (TOPMED)
C=0.1875/12 (PRJEB36033)
C=0.187755/92 (SGDP_PRJ)
C=0.203704/44 (Qatari)
C=0.246561/466 (HapMap)
C=0.260306/1304 (1000Genomes)
C=0.262277/1175 (Estonian)
C=0.269194/561 (HGDP_Stanford)
C=0.275/11 (GENOME_DK)
C=0.417333/6994 (TOMMO)
C=0.462799/1356 (KOREAN)
C=0.467249/856 (Korea1K)
HGVS:: NC_000007.14:g.138546075C>A, NC_000007.14:g.138546075C>T, NC_000007.13:g.138230820C>A, NC_000007.13:g.138230820C>T, NG_023286.1:g.90742C>A, NG_023286.1:g.90742C>T

Select item 155037817.

rs1550378 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:138518944 (GRCh38)
7:138203689 (GRCh37)
Canonical SPDI:: NC_000007.14:138518943:C:T
Gene:: TRIM24 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (HapMap)
T=0.000036/5 (GnomAD)
T=0.000045/12 (TOPMED)
T=0.000156/1 (1000Genomes)
T=0.000177/3 (TOMMO)
HGVS:: NC_000007.14:g.138518944C>T, NC_000007.13:g.138203689C>T, NG_023286.1:g.63611C>T

Select item 167320318.

rs1673203 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:138585912 (GRCh38)
7:138270657 (GRCh37)
Canonical SPDI:: NC_000007.14:138585911:G:A
Gene:: TRIM24 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.244712/7543 (ALFA)
A=0.195391/195 (GoNL)
G=0.2/6 (Siberian)
A=0.201609/777 (ALSPAC)
A=0.204153/757 (TWINSUK)
A=0.215356/115 (MGP)
A=0.217593/47 (Qatari)
A=0.223333/134 (NorthernSweden)
A=0.240402/263 (Daghestan)
A=0.245378/1407 (GoESP)
A=0.257403/36006 (GnomAD)
A=0.262828/69568 (TOPMED)
A=0.27131/62118 (GnomAD_exomes)
A=0.2741/30907 (ExAC)
A=0.277439/91 (HapMap)
A=0.299342/91 (FINRISK)
A=0.302902/1357 (Estonian)
A=0.338695/1696 (1000Genomes)
A=0.35/14 (GENOME_DK)
G=0.359477/110 (SGDP_PRJ)
A=0.428056/7173 (TOMMO)
G=0.452459/276 (Vietnamese)
A=0.462457/1355 (KOREAN)
A=0.465611/853 (Korea1K)
HGVS:: NC_000007.14:g.138585912G>A, NC_000007.13:g.138270657G>A, NG_023286.1:g.130579G>A, NM_003852.4:c.*961G>A, NM_015905.3:c.*961G>A, XM_024446981.2:c.*961G>A

Select item 167320419.

rs1673204 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C,G [Show Flanks]
Chromosome:: 7:138586093 (GRCh38)
7:138270838 (GRCh37)
Canonical SPDI:: NC_000007.14:138586092:T:A,NC_000007.14:138586092:T:C,NC_000007.14:138586092:T:G
Gene:: TRIM24 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.217255/5394 (ALFA)
G=0./0 (KOREAN)
T=0.096154/5 (Siberian)
T=0.175926/38 (Qatari)
T=0.218816/414 (HapMap)
T=0.22314/108 (SGDP_PRJ)
T=0.223719/31263 (GnomAD)
T=0.228333/137 (NorthernSweden)
T=0.230292/60956 (TOPMED)
T=0.25/10 (GENOME_DK)
T=0.257808/1291 (1000Genomes)
T=0.263363/1015 (ALSPAC)
T=0.268973/1205 (Estonian)
T=0.269539/269 (GoNL)
T=0.272114/1009 (TWINSUK)
C=0.437681/7335 (TOMMO)
T=0.476415/101 (Vietnamese)
C=0.478712/877 (Korea1K)
HGVS:: NC_000007.14:g.138586093T>A, NC_000007.14:g.138586093T>C, NC_000007.14:g.138586093T>G, NC_000007.13:g.138270838T>A, NC_000007.13:g.138270838T>C, NC_000007.13:g.138270838T>G, NG_023286.1:g.130760T>A, NG_023286.1:g.130760T>C, NG_023286.1:g.130760T>G, NM_003852.4:c.*1142T>A, NM_003852.4:c.*1142T>C, NM_003852.4:c.*1142T>G, NM_015905.3:c.*1142T>A, NM_015905.3:c.*1142T>C, NM_015905.3:c.*1142T>G, XM_024446981.2:c.*1142T>A, XM_024446981.2:c.*1142T>C, XM_024446981.2:c.*1142T>G

Select item 167320520.

rs1673205 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 7:138589442 (GRCh38)
7:138274187 (GRCh37)
Canonical SPDI:: NC_000007.14:138589441:T:A,NC_000007.14:138589441:T:G
Gene:: TRIM24 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.204238/3624 (ALFA)
T=0.125/5 (Siberian)
T=0.161323/161 (GoNL)
T=0.165283/637 (ALSPAC)
T=0.169364/628 (TWINSUK)
T=0.173333/104 (NorthernSweden)
T=0.199115/27892 (GnomAD)
T=0.203704/44 (Qatari)
T=0.205746/54459 (TOPMED)
T=0.209016/102 (SGDP_PRJ)
T=0.215152/71 (HapMap)
T=0.25692/1151 (Estonian)
T=0.275/11 (GENOME_DK)
T=0.277483/1390 (1000Genomes)
T=0.412662/6915 (TOMMO)
A=0.443396/94 (Vietnamese)
T=0.454949/1333 (KOREAN)
T=0.462336/847 (Korea1K)
HGVS:: NC_000007.14:g.138589442T>A, NC_000007.14:g.138589442T>G, NC_000007.13:g.138274187T>A, NC_000007.13:g.138274187T>G, NM_003852.4:c.*4491T>A, NM_003852.4:c.*4491T>G, NM_015905.3:c.*4491T>A, NM_015905.3:c.*4491T>G, XM_024446981.2:c.*4491T>A, XM_024446981.2:c.*4491T>G

<< First< Prev

Page of 2475

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Search results

Items: 1 to 20 of 49495

Display Settings:

Send to:

Supplemental Content

Find related data

Search details

Recent activity