RAD51B - SNP

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Select item 7658991.

rs765899 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:68497029 (GRCh38)
14:68963746 (GRCh37)
Canonical SPDI:: NC_000014.9:68497028:C:T
Gene:: RAD51B (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.393086/118488 (ALFA)
T=0.258065/16 (PRJEB36033)
T=0.29704/562 (HapMap)
T=0.302432/23799 (PAGE_STUDY)
C=0.309524/13 (Siberian)
T=0.31441/576 (Korea1K)
C=0.315029/109 (SGDP_PRJ)
T=0.320579/44906 (GnomAD)
T=0.325597/954 (KOREAN)
T=0.325751/86223 (TOPMED)
T=0.32987/254 (PRJEB37584)
T=0.344569/184 (MGP)
T=0.35634/1785 (1000Genomes)
T=0.375752/375 (GoNL)
T=0.376483/1396 (TWINSUK)
T=0.376637/6312 (TOMMO)
T=0.388889/84 (Qatari)
T=0.39097/814 (HGDP_Stanford)
T=0.393586/80715 (GENOGRAPHIC)
T=0.401401/1547 (ALSPAC)
T=0.44308/1985 (Estonian)
T=0.446667/268 (NorthernSweden)
T=0.45/18 (GENOME_DK)
C=0.462264/98 (Vietnamese)
HGVS:: NC_000014.9:g.68497029C>T, NC_000014.8:g.68963746C>T, NG_023267.2:g.682251C>T

PubMed

Select item 9617002.

rs961700 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 14:67864720 (GRCh38)
14:68331437 (GRCh37)
Canonical SPDI:: NC_000014.9:67864719:G:A,NC_000014.9:67864719:G:C
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.386436/97045 (ALFA)
A=0.073791/58 (PRJEB37584)
A=0.078704/17 (Vietnamese)
A=0.094487/1584 (TOMMO)
A=0.097707/179 (Korea1K)
A=0.102048/299 (KOREAN)
A=0.3/12 (GENOME_DK)
A=0.346658/1736 (1000Genomes)
A=0.351562/1575 (Estonian)
G=0.357143/90 (SGDP_PRJ)
A=0.359125/673 (HapMap)
A=0.382405/78422 (GENOGRAPHIC)
A=0.385/231 (NorthernSweden)
A=0.398876/213 (MGP)
G=0.4/12 (Siberian)
A=0.400755/1486 (TWINSUK)
A=0.40481/404 (GoNL)
A=0.408926/1576 (ALSPAC)
A=0.411394/108892 (TOPMED)
A=0.417041/58339 (GnomAD)
A=0.444444/96 (Qatari)
HGVS:: NC_000014.9:g.67864720G>A, NC_000014.9:g.67864720G>C, NC_000014.8:g.68331437G>A, NC_000014.8:g.68331437G>C, NG_023267.2:g.49942G>A, NG_023267.2:g.49942G>C

PubMed LitVar

Select item 9997373.

rs999737 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 14:68567965 (GRCh38)
14:69034682 (GRCh37)
Canonical SPDI:: NC_000014.9:68567964:C:A,NC_000014.9:68567964:C:T
Gene:: RAD51B (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.214297/73921 (ALFA)
T=0.000342/1 (KOREAN)
T=0.000546/1 (Korea1K)
T=0.069444/15 (Qatari)
T=0.090411/7115 (PAGE_STUDY)
T=0.091661/459 (1000Genomes)
T=0.093796/127 (HapMap)
T=0.099808/208 (HGDP_Stanford)
T=0.149669/39616 (TOPMED)
T=0.160408/22462 (GnomAD)
T=0.2/8 (PRJEB36033)
T=0.239482/888 (TWINSUK)
T=0.240625/1078 (Estonian)
T=0.246493/246 (GoNL)
T=0.247535/954 (ALSPAC)
T=0.273333/164 (NorthernSweden)
T=0.325/13 (GENOME_DK)
C=0.346154/9 (Siberian)
C=0.488095/41 (SGDP_PRJ)
HGVS:: NC_000014.9:g.68567965C>A, NC_000014.9:g.68567965C>T, NC_000014.8:g.69034682C>A, NC_000014.8:g.69034682C>T, NG_023267.2:g.753187C>A, NG_023267.2:g.753187C>T

PubMed LitVar

Select item 14749394.

rs1474939 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 14:67864958 (GRCh38)
14:68331675 (GRCh37)
Canonical SPDI:: NC_000014.9:67864957:A:C,NC_000014.9:67864957:A:G,NC_000014.9:67864957:A:T
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0./0 (GENOME_DK)
G=0./0 (KOREAN)
A=0./0 (Qatari)
A=0.001/1 (GoNL)
A=0.00717/4 (SGDP_PRJ)
A=0.01031/6 (NorthernSweden)
A=0.03124/409 (TOMMO)
T=0.05431/29 (MGP)
A=0.0939/120 (Korea1K)
A=0.12149/778 (1000Genomes)
A=0.35/14 (Siberian)
HGVS:: NC_000014.9:g.67864958A>C, NC_000014.9:g.67864958A>G, NC_000014.9:g.67864958A>T, NC_000014.8:g.68331675A>C, NC_000014.8:g.68331675A>G, NC_000014.8:g.68331675A>T, NG_023267.2:g.50180A>C, NG_023267.2:g.50180A>G, NG_023267.2:g.50180A>T

Select item 15413905.

rs1541390 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 14:68513212 (GRCh38)
14:68979929 (GRCh37)
Canonical SPDI:: NC_000014.9:68513211:A:G,NC_000014.9:68513211:A:T
Gene:: RAD51B (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.214443/32308 (ALFA)
G=0.151667/91 (NorthernSweden)
G=0.173913/8 (PRJEB36033)
G=0.188116/725 (ALSPAC)
G=0.189062/847 (Estonian)
G=0.196393/196 (GoNL)
G=0.20712/768 (TWINSUK)
G=0.215398/44173 (GENOGRAPHIC)
G=0.225/9 (GENOME_DK)
G=0.233966/32766 (GnomAD)
G=0.236111/51 (Qatari)
G=0.241214/151 (Chileans)
G=0.246024/65120 (TOPMED)
G=0.303911/575 (HapMap)
G=0.304223/634 (HGDP_Stanford)
G=0.306059/1533 (1000Genomes)
A=0.388889/112 (SGDP_PRJ)
G=0.401869/86 (Vietnamese)
A=0.427304/1252 (KOREAN)
A=0.428571/6 (Siberian)
A=0.435044/797 (Korea1K)
A=0.49133/8235 (TOMMO)
HGVS:: NC_000014.9:g.68513212A>G, NC_000014.9:g.68513212A>T, NC_000014.8:g.68979929A>G, NC_000014.8:g.68979929A>T, NG_023267.2:g.698434A>G, NG_023267.2:g.698434A>T

Select item 20745626.

rs2074562 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 14:68467973 (GRCh38)
14:68934690 (GRCh37)
Canonical SPDI:: NC_000014.9:68467972:A:G,NC_000014.9:68467972:A:T
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.346349/80991 (ALFA)
G=0.003745/2 (MGP)
A=0.125/4 (PRJEB36033)
A=0.255981/107 (SGDP_PRJ)
A=0.306095/1135 (TWINSUK)
A=0.309524/13 (Siberian)
A=0.316633/316 (GoNL)
A=0.325/13 (GENOME_DK)
A=0.327137/86590 (TOPMED)
A=0.334977/1291 (ALSPAC)
A=0.340162/69759 (GENOGRAPHIC)
A=0.346753/267 (PRJEB37584)
A=0.349345/640 (Korea1K)
A=0.350132/27554 (PAGE_STUDY)
A=0.35631/672 (HapMap)
A=0.365529/1071 (KOREAN)
A=0.38817/1739 (Estonian)
A=0.389913/1953 (1000Genomes)
A=0.393519/85 (Qatari)
A=0.401667/241 (NorthernSweden)
A=0.405584/6798 (TOMMO)
A=0.424184/884 (HGDP_Stanford)
G=0.4377/274 (Chileans)
G=0.462264/98 (Vietnamese)
HGVS:: NC_000014.9:g.68467973A>G, NC_000014.9:g.68467973A>T, NC_000014.8:g.68934690A>G, NC_000014.8:g.68934690A>T, NG_023267.2:g.653195A>G, NG_023267.2:g.653195A>T

Select item 20745637.

rs2074563 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 14:68468395 (GRCh38)
14:68935112 (GRCh37)
Canonical SPDI:: NC_000014.9:68468394:G:A,NC_000014.9:68468394:G:C,NC_000014.9:68468394:G:T
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.383431/94742 (ALFA)
T=0./0 (KOREAN)
A=0.258786/162 (Chileans)
A=0.328704/71 (Qatari)
G=0.356287/119 (SGDP_PRJ)
G=0.366667/11 (Siberian)
G=0.381004/698 (Korea1K)
A=0.385772/385 (GoNL)
A=0.386611/1490 (ALSPAC)
A=0.391386/209 (MGP)
G=0.392765/304 (PRJEB37584)
A=0.397545/1781 (Estonian)
A=0.401667/241 (NorthernSweden)
A=0.401834/1490 (TWINSUK)
G=0.423491/7098 (TOMMO)
A=0.438164/2194 (1000Genomes)
A=0.440874/116695 (TOPMED)
A=0.442308/92 (Vietnamese)
A=0.450621/63095 (GnomAD)
A=0.474074/896 (HapMap)
A=0.480831/37826 (PAGE_STUDY)
G=0.5/20 (GENOME_DK)
HGVS:: NC_000014.9:g.68468395G>A, NC_000014.9:g.68468395G>C, NC_000014.9:g.68468395G>T, NC_000014.8:g.68935112G>A, NC_000014.8:g.68935112G>C, NC_000014.8:g.68935112G>T, NG_023267.2:g.653617G>A, NG_023267.2:g.653617G>C, NG_023267.2:g.653617G>T

Select item 20745658.

rs2074565 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 14:68477430 (GRCh38)
14:68944147 (GRCh37)
Canonical SPDI:: NC_000014.9:68477429:T:C,NC_000014.9:68477429:T:G
Gene:: RAD51B (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.383662/30043 (ALFA)
G=0.102996/55 (MGP)
G=0.288889/26 (PRJEB36033)
G=0.337963/73 (Qatari)
T=0.365269/122 (SGDP_PRJ)
T=0.366667/11 (Siberian)
T=0.380459/697 (Korea1K)
G=0.38477/384 (GoNL)
G=0.386871/1491 (ALSPAC)
G=0.397098/1779 (Estonian)
G=0.398273/830 (HGDP_Stanford)
G=0.401564/1489 (TWINSUK)
T=0.402048/1178 (KOREAN)
G=0.406667/244 (NorthernSweden)
G=0.421299/2110 (1000Genomes)
T=0.423273/7093 (TOMMO)
G=0.427425/113135 (TOPMED)
G=0.437978/61218 (GnomAD)
G=0.439252/94 (Vietnamese)
G=0.455556/861 (HapMap)
T=0.5/20 (GENOME_DK)
HGVS:: NC_000014.9:g.68477430T>C, NC_000014.9:g.68477430T>G, NC_000014.8:g.68944147T>C, NC_000014.8:g.68944147T>G, NG_023267.2:g.662652T>C, NG_023267.2:g.662652T>G

Select item 25888089.

rs2588808 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 14:68193464 (GRCh38)
14:68660181 (GRCh37)
Canonical SPDI:: NC_000014.9:68193463:A:C,NC_000014.9:68193463:A:G,NC_000014.9:68193463:A:T
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.16046/10427 (ALFA)
T=0./0 (KOREAN)
A=0.013889/3 (Vietnamese)
A=0.022861/383 (TOMMO)
A=0.056667/34 (NorthernSweden)
A=0.075/3 (GENOME_DK)
A=0.102232/458 (Estonian)
A=0.107143/6 (Siberian)
A=0.124242/41 (HapMap)
A=0.124549/69 (SGDP_PRJ)
A=0.140537/704 (1000Genomes)
A=0.144289/144 (GoNL)
A=0.156149/579 (TWINSUK)
A=0.157767/22100 (GnomAD)
A=0.158018/609 (ALSPAC)
A=0.163316/43228 (TOPMED)
A=0.25/16 (PRJEB36033)
A=0.263889/57 (Qatari)
HGVS:: NC_000014.9:g.68193464A>C, NC_000014.9:g.68193464A>G, NC_000014.9:g.68193464A>T, NC_000014.8:g.68660181A>C, NC_000014.8:g.68660181A>G, NC_000014.8:g.68660181A>T, NG_023267.2:g.378686A>C, NG_023267.2:g.378686A>G, NG_023267.2:g.378686A>T

Select item 258880910.

rs2588809 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C,G [Show Flanks]
Chromosome:: 14:68193711 (GRCh38)
14:68660428 (GRCh37)
Canonical SPDI:: NC_000014.9:68193710:T:A,NC_000014.9:68193710:T:C,NC_000014.9:68193710:T:G
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.177611/7411 (ALFA)
G=0./0 (KOREAN)
T=0.020253/16 (PRJEB37584)
T=0.022861/383 (TOMMO)
T=0.023148/5 (Vietnamese)
T=0.063333/38 (NorthernSweden)
T=0.1/4 (GENOME_DK)
T=0.107589/482 (Estonian)
T=0.141221/74 (SGDP_PRJ)
T=0.142857/8 (Siberian)
T=0.143287/143 (GoNL)
T=0.150234/579 (ALSPAC)
T=0.155609/577 (TWINSUK)
T=0.162162/12 (PRJEB36033)
T=0.18832/943 (1000Genomes)
T=0.201568/28236 (GnomAD)
T=0.207836/55012 (TOPMED)
T=0.208955/392 (HapMap)
T=0.210626/16575 (PAGE_STUDY)
T=0.342593/74 (Qatari)
HGVS:: NC_000014.9:g.68193711T>A, NC_000014.9:g.68193711T>C, NC_000014.9:g.68193711T>G, NC_000014.8:g.68660428T>A, NC_000014.8:g.68660428T>C, NC_000014.8:g.68660428T>G, NG_023267.2:g.378933T>A, NG_023267.2:g.378933T>C, NG_023267.2:g.378933T>G

PubMed LitVar

Select item 284232011.

rs2842320 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:68477356 (GRCh38)
14:68944073 (GRCh37)
Canonical SPDI:: NC_000014.9:68477355:A:G
Gene:: RAD51B (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.181249/13059 (ALFA)
G=0.018014/302 (TOMMO)
G=0.031659/58 (Korea1K)
G=0.032407/7 (Vietnamese)
G=0.037645/110 (KOREAN)
G=0.1/4 (GENOME_DK)
G=0.10582/200 (HapMap)
G=0.112117/561 (1000Genomes)
G=0.113244/236 (HGDP_Stanford)
G=0.116667/70 (NorthernSweden)
G=0.137054/614 (Estonian)
G=0.14843/39288 (TOPMED)
G=0.149864/20999 (GnomAD)
G=0.189154/729 (ALSPAC)
G=0.194389/194 (GoNL)
G=0.196332/728 (TWINSUK)
G=0.222222/48 (Qatari)
G=0.375/36 (PRJEB36033)
A=0.414894/39 (SGDP_PRJ)
A=0.428571/6 (Siberian)
HGVS:: NC_000014.9:g.68477356A>G, NC_000014.8:g.68944073A>G, NG_023267.2:g.662578A>G

PubMed

Select item 490253012.

rs4902530 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:67885606 (GRCh38)
14:68352323 (GRCh37)
Canonical SPDI:: NC_000014.9:67885605:A:G
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.034621/654 (ALFA)
G=0.005357/24 (Estonian)
G=0.007014/7 (GoNL)
G=0.01/6 (NorthernSweden)
G=0.011676/45 (ALSPAC)
G=0.014293/53 (TWINSUK)
G=0.025/1 (GENOME_DK)
G=0.043269/9 (HapMap)
G=0.053954/7567 (GnomAD)
G=0.057301/15167 (TOPMED)
G=0.059498/109 (Korea1K)
G=0.060185/13 (Vietnamese)
G=0.063168/1059 (TOMMO)
G=0.066553/195 (KOREAN)
G=0.071486/358 (1000Genomes)
G=0.092593/20 (Qatari)
A=0.47619/20 (SGDP_PRJ)
A=0.5/1 (Siberian)
HGVS:: NC_000014.9:g.67885606A>G, NC_000014.8:g.68352323A>G, NG_023267.2:g.70828A>G

Select item 490253113.

rs4902531 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 14:67887435 (GRCh38)
14:68354152 (GRCh37)
Canonical SPDI:: NC_000014.9:67887434:C:A,NC_000014.9:67887434:C:T
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.011157/199 (ALFA)
T=0.00558/25 (Estonian)
T=0.008016/8 (GoNL)
T=0.01/6 (NorthernSweden)
T=0.011676/45 (ALSPAC)
T=0.014293/53 (TWINSUK)
T=0.025/1 (GENOME_DK)
T=0.059498/109 (Korea1K)
T=0.063203/1059 (TOMMO)
T=0.063462/8885 (GnomAD)
T=0.067235/197 (KOREAN)
T=0.067479/17861 (TOPMED)
T=0.070755/15 (Vietnamese)
T=0.085884/430 (1000Genomes)
T=0.104294/34 (HapMap)
T=0.106481/23 (Qatari)
C=0.48/24 (SGDP_PRJ)
C=0.5/1 (Siberian)
HGVS:: NC_000014.9:g.67887435C>A, NC_000014.9:g.67887435C>T, NC_000014.8:g.68354152C>A, NC_000014.8:g.68354152C>T, NG_023267.2:g.72657C>A, NG_023267.2:g.72657C>T

Select item 500409014.

rs5004090 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:68477528 (GRCh38)
14:68944245 (GRCh37)
Canonical SPDI:: NC_000014.9:68477527:T:C
Gene:: RAD51B (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.411187/8042 (ALFA)
C=0.337963/73 (Qatari)
T=0.366667/11 (Siberian)
T=0.366667/121 (SGDP_PRJ)
T=0.380459/697 (Korea1K)
C=0.382022/204 (MGP)
C=0.38477/384 (GoNL)
C=0.38713/1492 (ALSPAC)
C=0.397545/1781 (Estonian)
C=0.401294/1488 (TWINSUK)
C=0.401667/241 (NorthernSweden)
T=0.401706/1177 (KOREAN)
C=0.421143/2109 (1000Genomes)
T=0.423066/7091 (TOMMO)
C=0.427515/113159 (TOPMED)
C=0.438254/61324 (GnomAD)
T=0.5/20 (GENOME_DK)
HGVS:: NC_000014.9:g.68477528T>C, NC_000014.8:g.68944245T>C, NG_023267.2:g.662750T>C

Select item 800608915.

rs8006089 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 14:67823803 (GRCh38)
14:68290520 (GRCh37)
Canonical SPDI:: NC_000014.9:67823802:T:A,NC_000014.9:67823802:T:G
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.34352/47135 (ALFA)
G=0.163812/2745 (TOMMO)
G=0.17372/509 (KOREAN)
G=0.179585/329 (Korea1K)
G=0.214058/134 (Chileans)
G=0.25/10 (GENOME_DK)
G=0.314179/1573 (1000Genomes)
G=0.33192/1487 (Estonian)
G=0.335624/635 (HapMap)
G=0.363333/218 (NorthernSweden)
G=0.368518/97543 (TOPMED)
G=0.375/81 (Qatari)
T=0.379562/104 (SGDP_PRJ)
T=0.384615/10 (Siberian)
HGVS:: NC_000014.9:g.67823803T>A, NC_000014.9:g.67823803T>G, NC_000014.8:g.68290520T>A, NC_000014.8:g.68290520T>G, NG_023267.2:g.9025T>A, NG_023267.2:g.9025T>G

Select item 801139316.

rs8011393 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 14:67825181 (GRCh38)
14:68291898 (GRCh37)
Canonical SPDI:: NC_000014.9:67825180:C:A,NC_000014.9:67825180:C:T
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.32466/5914 (ALFA)
T=0.100983/185 (Korea1K)
T=0.103058/1727 (TOMMO)
T=0.107803/315 (KOREAN)
T=0.25/10 (GENOME_DK)
T=0.254528/1275 (1000Genomes)
T=0.273292/88 (HapMap)
T=0.291667/63 (Qatari)
T=0.32427/85831 (TOPMED)
T=0.329688/1477 (Estonian)
T=0.331022/45926 (GnomAD)
T=0.363333/218 (NorthernSweden)
T=0.364347/1351 (TWINSUK)
T=0.365731/365 (GoNL)
T=0.366373/1412 (ALSPAC)
C=0.375/84 (SGDP_PRJ)
C=0.375/9 (Siberian)
HGVS:: NC_000014.9:g.67825181C>A, NC_000014.9:g.67825181C>T, NC_000014.8:g.68291898C>A, NC_000014.8:g.68291898C>T, NG_023267.2:g.10403C>A, NG_023267.2:g.10403C>T

Select item 801169017.

rs8011690 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:67825190 (GRCh38)
14:68291907 (GRCh37)
Canonical SPDI:: NC_000014.9:67825189:G:A
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.354195/29814 (ALFA)
A=0.104651/9 (HapMap)
A=0.163434/2739 (TOMMO)
A=0.17372/509 (KOREAN)
A=0.179039/328 (Korea1K)
A=0.25/10 (GENOME_DK)
A=0.330134/1479 (Estonian)
A=0.342598/1716 (1000Genomes)
G=0.360714/101 (SGDP_PRJ)
A=0.363333/218 (NorthernSweden)
A=0.365696/1356 (TWINSUK)
A=0.367735/367 (GoNL)
A=0.367929/1418 (ALSPAC)
A=0.384259/83 (Qatari)
G=0.384615/10 (Siberian)
A=0.3932/104076 (TOPMED)
A=0.39696/54998 (GnomAD)
HGVS:: NC_000014.9:g.67825190G>A, NC_000014.8:g.68291907G>A, NG_023267.2:g.10412G>A

Select item 801700718.

rs8017007 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 14:67886188 (GRCh38)
14:68352905 (GRCh37)
Canonical SPDI:: NC_000014.9:67886187:G:A,NC_000014.9:67886187:G:T
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.263167/3128 (ALFA)
A=0.079439/17 (Vietnamese)
A=0.081357/1364 (TOMMO)
A=0.093886/172 (Korea1K)
A=0.100341/294 (KOREAN)
A=0.3/12 (GENOME_DK)
G=0.344961/89 (SGDP_PRJ)
A=0.351562/1575 (Estonian)
A=0.356964/1788 (1000Genomes)
G=0.366667/11 (Siberian)
A=0.37/222 (NorthernSweden)
A=0.400755/1486 (TWINSUK)
A=0.406814/406 (GoNL)
A=0.409704/1579 (ALSPAC)
A=0.421187/111484 (TOPMED)
A=0.426759/59719 (GnomAD)
A=0.444444/96 (Qatari)
HGVS:: NC_000014.9:g.67886188G>A, NC_000014.9:g.67886188G>T, NC_000014.8:g.68352905G>A, NC_000014.8:g.68352905G>T, NG_023267.2:g.71410G>A, NG_023267.2:g.71410G>T

Select item 801730419.

rs8017304 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:68318360 (GRCh38)
14:68785077 (GRCh37)
Canonical SPDI:: NC_000014.9:68318359:G:A
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: not-provided
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.388843/62694 (ALFA)
G=0.277778/15 (Siberian)
G=0.3/12 (GENOME_DK)
G=0.303828/127 (SGDP_PRJ)
G=0.315/189 (NorthernSweden)
G=0.345089/1546 (Estonian)
G=0.347431/1339 (ALSPAC)
G=0.360302/1336 (TWINSUK)
G=0.38978/389 (GoNL)
A=0.407692/318 (PRJEB37584)
A=0.411572/754 (Korea1K)
A=0.420819/1233 (KOREAN)
A=0.447674/847 (HapMap)
G=0.454545/30 (PRJEB36033)
G=0.464277/64931 (GnomAD)
A=0.470913/37058 (PAGE_STUDY)
A=0.471963/101 (Vietnamese)
G=0.47516/125770 (TOPMED)
A=0.476852/103 (Qatari)
A=0.49041/8219 (TOMMO)
A=0.49594/2484 (1000Genomes)
HGVS:: NC_000014.9:g.68318360G>A, NC_000014.8:g.68785077G>A, NG_023267.2:g.503582G>A

PubMed

Select item 1012964620.

rs10129646 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:68291858 (GRCh38)
14:68758575 (GRCh37)
Canonical SPDI:: NC_000014.9:68291857:T:C
Gene:: RAD51B (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.023989/1008 (ALFA)
C=0.001002/1 (GoNL)
C=0.002076/8 (ALSPAC)
C=0.002427/9 (TWINSUK)
C=0.002455/11 (Estonian)
C=0.017652/3620 (GENOGRAPHIC)
C=0.024345/13 (MGP)
C=0.025/1 (GENOME_DK)
C=0.037383/8 (Vietnamese)
C=0.041814/10473 (GnomAD_exomes)
C=0.046602/5635 (ExAC)
C=0.074074/16 (Qatari)
C=0.109795/1428 (GoESP)
C=0.110836/1858 (TOMMO)
C=0.111425/15612 (GnomAD)
C=0.12246/32414 (TOPMED)
C=0.134825/247 (Korea1K)
C=0.142723/715 (1000Genomes)
C=0.147502/431 (KOREAN)
C=0.200898/358 (HapMap)
T=0.449153/53 (SGDP_PRJ)
T=0.5/2 (Siberian)
HGVS:: NC_000014.9:g.68291858T>C, NC_000014.8:g.68758575T>C, NG_023267.2:g.477080T>C

PubMed

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