ANKRD22 - SNP

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Select item 9627711.

rs962771 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 10:88833935 (GRCh38)
10:90593692 (GRCh37)
Canonical SPDI:: NC_000010.11:88833934:C:A,NC_000010.11:88833934:C:T
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.295987/10401 (ALFA)
T=0.107477/23 (Vietnamese)
T=0.15802/463 (KOREAN)
T=0.162118/297 (Korea1K)
T=0.185304/116 (Chileans)
T=0.209604/3513 (TOMMO)
T=0.268519/58 (Qatari)
T=0.325651/325 (GoNL)
T=0.333385/1670 (1000Genomes)
T=0.333873/1238 (TWINSUK)
T=0.342501/1320 (ALSPAC)
T=0.36582/96829 (TOPMED)
T=0.366667/220 (NorthernSweden)
T=0.368922/698 (HapMap)
T=0.382308/53514 (GnomAD)
T=0.38817/1739 (Estonian)
C=0.4/100 (SGDP_PRJ)
C=0.461538/12 (Siberian)
T=0.475/19 (GENOME_DK)
HGVS:: NC_000010.11:g.88833935C>A, NC_000010.11:g.88833935C>T, NC_000010.10:g.90593692C>A, NC_000010.10:g.90593692C>T

Select item 9627722.

rs962772 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:88833859 (GRCh38)
10:90593616 (GRCh37)
Canonical SPDI:: NC_000010.11:88833858:C:T
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.374219/7069 (ALFA)
T=0.098131/21 (Vietnamese)
T=0.15802/463 (KOREAN)
T=0.162118/297 (Korea1K)
T=0.209604/3513 (TOMMO)
T=0.273148/59 (Qatari)
T=0.325651/325 (GoNL)
T=0.334142/1239 (TWINSUK)
T=0.335728/1681 (1000Genomes)
T=0.34302/1322 (ALSPAC)
T=0.366667/220 (NorthernSweden)
T=0.367751/97340 (TOPMED)
T=0.384226/53774 (GnomAD)
T=0.388393/1740 (Estonian)
C=0.400794/101 (SGDP_PRJ)
C=0.461538/12 (Siberian)
T=0.475/19 (GENOME_DK)
HGVS:: NC_000010.11:g.88833859C>T, NC_000010.10:g.90593616C>T

Select item 10290243.

rs1029024 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 10:88828778 (GRCh38)
10:90588535 (GRCh37)
Canonical SPDI:: NC_000010.11:88828777:G:A,NC_000010.11:88828777:G:C,NC_000010.11:88828777:G:T
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.238513/62030 (ALFA)
T=0./0 (KOREAN)
G=0.12/6 (Siberian)
G=0.134051/2247 (TOMMO)
G=0.15566/33 (Vietnamese)
G=0.16/80 (SGDP_PRJ)
G=0.199782/366 (Korea1K)
G=0.2/158 (PRJEB37584)
G=0.21737/453 (HGDP_Stanford)
G=0.228571/16 (PRJEB36033)
G=0.235268/1054 (Estonian)
G=0.25/150 (NorthernSweden)
G=0.264529/264 (GoNL)
G=0.287037/62 (Qatari)
G=0.30762/1541 (1000Genomes)
G=0.314471/44026 (GnomAD)
G=0.32328/611 (HapMap)
G=0.32376/85696 (TOPMED)
G=0.35/14 (GENOME_DK)
G=0.355068/27919 (PAGE_STUDY)
HGVS:: NC_000010.11:g.88828778G>A, NC_000010.11:g.88828778G>C, NC_000010.11:g.88828778G>T, NC_000010.10:g.90588535G>A, NC_000010.10:g.90588535G>C, NC_000010.10:g.90588535G>T

Select item 10290254.

rs1029025 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:88828404 (GRCh38)
10:90588161 (GRCh37)
Canonical SPDI:: NC_000010.11:88828403:C:T
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.278137/5254 (ALFA)
C=0.12/6 (Siberian)
C=0.134015/2246 (TOMMO)
C=0.16/80 (SGDP_PRJ)
C=0.174744/512 (KOREAN)
C=0.199782/366 (Korea1K)
C=0.237277/1063 (Estonian)
C=0.25/150 (NorthernSweden)
T=0.252809/135 (MGP)
C=0.265531/265 (GoNL)
C=0.287037/62 (Qatari)
C=0.30762/1541 (1000Genomes)
C=0.315139/44047 (GnomAD)
C=0.323733/85689 (TOPMED)
C=0.35/14 (GENOME_DK)
HGVS:: NC_000010.11:g.88828404C>T, NC_000010.10:g.90588161C>T

Select item 11476015.

rs1147601 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:88848481 (GRCh38)
10:90608238 (GRCh37)
Canonical SPDI:: NC_000010.11:88848480:A:G
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.212454/44614 (ALFA)
G=0.028037/6 (Vietnamese)
G=0.030459/89 (KOREAN)
G=0.033297/61 (Korea1K)
G=0.075908/1272 (TOMMO)
G=0.102236/64 (Chileans)
G=0.109691/206 (HapMap)
G=0.111111/24 (Qatari)
G=0.112284/234 (HGDP_Stanford)
G=0.117895/590 (1000Genomes)
G=0.153085/40520 (TOPMED)
G=0.173602/24306 (GnomAD)
G=0.178697/203 (Daghestan)
G=0.23247/862 (TWINSUK)
G=0.237156/914 (ALSPAC)
G=0.241379/14 (PRJEB36033)
G=0.243487/243 (GoNL)
G=0.268333/161 (NorthernSweden)
G=0.275893/1236 (Estonian)
G=0.425/17 (GENOME_DK)
A=0.454545/10 (Siberian)
A=0.484615/63 (SGDP_PRJ)
HGVS:: NC_000010.11:g.88848481A>G, NC_000010.10:g.90608238A>G

LitVar

Select item 12145496.

rs1214549 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:88832139 (GRCh38)
10:90591896 (GRCh37)
Canonical SPDI:: NC_000010.11:88832138:T:C
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.326513/42096 (ALFA)
C=0.011236/6 (MGP)
C=0.041667/9 (Vietnamese)
C=0.057495/168 (KOREAN)
C=0.06714/123 (Korea1K)
C=0.105103/1762 (TOMMO)
C=0.236111/51 (Qatari)
C=0.247189/1238 (1000Genomes)
C=0.2634/20728 (PAGE_STUDY)
C=0.267327/54 (HapMap)
C=0.303079/80222 (TOPMED)
C=0.319639/319 (GoNL)
C=0.323331/45278 (GnomAD)
C=0.32767/1215 (TWINSUK)
C=0.335236/1292 (ALSPAC)
C=0.38/228 (NorthernSweden)
C=0.392188/1757 (Estonian)
T=0.440594/89 (SGDP_PRJ)
C=0.45/18 (GENOME_DK)
T=0.461538/12 (Siberian)
HGVS:: NC_000010.11:g.88832139T>C, NC_000010.10:g.90591896T>C

Select item 12145507.

rs1214550 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 10:88832350 (GRCh38)
10:90592107 (GRCh37)
Canonical SPDI:: NC_000010.11:88832349:G:A,NC_000010.11:88832349:G:T
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.317965/60269 (ALFA)
A=0.070093/15 (Vietnamese)
A=0.104437/306 (KOREAN)
A=0.112991/207 (Korea1K)
A=0.15625/10 (PRJEB36033)
A=0.165511/2774 (TOMMO)
A=0.243985/507 (HGDP_Stanford)
A=0.268519/58 (Qatari)
A=0.307776/1541 (1000Genomes)
A=0.318637/318 (GoNL)
A=0.329288/1221 (TWINSUK)
A=0.335631/633 (HapMap)
A=0.337312/1300 (ALSPAC)
A=0.353999/93700 (TOPMED)
A=0.361667/217 (NorthernSweden)
A=0.37433/1677 (Estonian)
G=0.409483/95 (SGDP_PRJ)
A=0.45/18 (GENOME_DK)
G=0.458333/11 (Siberian)
HGVS:: NC_000010.11:g.88832350G>A, NC_000010.11:g.88832350G>T, NC_000010.10:g.90592107G>A, NC_000010.10:g.90592107G>T

Select item 12145518.

rs1214551 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C,G [Show Flanks]
Chromosome:: 10:88833172 (GRCh38)
10:90592929 (GRCh37)
Canonical SPDI:: NC_000010.11:88833171:T:A,NC_000010.11:88833171:T:C,NC_000010.11:88833171:T:G
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.292522/40058 (ALFA)
T=0.042453/9 (Vietnamese)
T=0.090102/264 (KOREAN)
T=0.096185/1612 (TOMMO)
T=0.121212/64 (SGDP_PRJ)
T=0.134615/7 (Siberian)
T=0.140212/265 (HapMap)
T=0.161149/807 (1000Genomes)
T=0.199074/43 (Qatari)
T=0.203345/231 (Daghestan)
T=0.222857/58988 (TOPMED)
T=0.251116/1125 (Estonian)
T=0.261667/157 (NorthernSweden)
T=0.275/11 (GENOME_DK)
T=0.338677/338 (GoNL)
HGVS:: NC_000010.11:g.88833172T>A, NC_000010.11:g.88833172T>C, NC_000010.11:g.88833172T>G, NC_000010.10:g.90592929T>A, NC_000010.10:g.90592929T>C, NC_000010.10:g.90592929T>G

Select item 12145529.

rs1214552 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:88834869 (GRCh38)
10:90594626 (GRCh37)
Canonical SPDI:: NC_000010.11:88834868:C:G,NC_000010.11:88834868:C:T
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.220889/2633 (ALFA)
G=0.0625/13 (Vietnamese)
G=0.106143/311 (KOREAN)
G=0.114083/209 (Korea1K)
G=0.165522/2774 (TOMMO)
G=0.268519/58 (Qatari)
G=0.308401/1544 (1000Genomes)
G=0.319639/319 (GoNL)
G=0.330065/101 (HapMap)
G=0.330097/1224 (TWINSUK)
G=0.337831/1302 (ALSPAC)
G=0.3548/93912 (TOPMED)
G=0.371592/51959 (GnomAD)
G=0.38/228 (NorthernSweden)
G=0.392411/1758 (Estonian)
C=0.409483/95 (SGDP_PRJ)
G=0.45/18 (GENOME_DK)
C=0.461538/12 (Siberian)
HGVS:: NC_000010.11:g.88834869C>G, NC_000010.11:g.88834869C>T, NC_000010.10:g.90594626C>G, NC_000010.10:g.90594626C>T

Select item 121455310.

rs1214553 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C,G [Show Flanks]
Chromosome:: 10:88836885 (GRCh38)
10:90596642 (GRCh37)
Canonical SPDI:: NC_000010.11:88836884:T:A,NC_000010.11:88836884:T:C,NC_000010.11:88836884:T:G
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.002832/51 (ALFA)
T=0./0 (GENOME_DK)
A=0./0 (KOREAN)
T=0./0 (Korea1K)
T=0./0 (NorthernSweden)
T=0./0 (Qatari)
T=0./0 (Siberian)
T=0./0 (Vietnamese)
T=0.000035/1 (TOMMO)
T=0.001116/5 (Estonian)
T=0.003258/457 (GnomAD)
T=0.003435/17 (1000Genomes)
T=0.003612/956 (TOPMED)
T=0.004008/4 (GoNL)
T=0.004045/15 (TWINSUK)
T=0.004152/16 (ALSPAC)
T=0.006135/2 (HapMap)
T=0.008961/5 (SGDP_PRJ)
HGVS:: NC_000010.11:g.88836885T>A, NC_000010.11:g.88836885T>C, NC_000010.11:g.88836885T>G, NC_000010.10:g.90596642T>A, NC_000010.10:g.90596642T>C, NC_000010.10:g.90596642T>G

Select item 121455411.

rs1214554 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:88837102 (GRCh38)
10:90596859 (GRCh37)
Canonical SPDI:: NC_000010.11:88837101:G:A
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.337155/83373 (ALFA)
A=0.096154/20 (Vietnamese)
A=0.157679/462 (KOREAN)
A=0.16285/128 (PRJEB37584)
A=0.16321/299 (Korea1K)
A=0.209994/3519 (TOMMO)
A=0.268519/58 (Qatari)
A=0.325651/325 (GoNL)
A=0.334412/1240 (TWINSUK)
A=0.337601/1691 (1000Genomes)
A=0.342761/1321 (ALSPAC)
A=0.365902/28795 (PAGE_STUDY)
A=0.366667/220 (NorthernSweden)
A=0.371008/98202 (TOPMED)
A=0.373457/121 (HapMap)
A=0.387173/54167 (GnomAD)
A=0.38817/1739 (Estonian)
G=0.396/99 (SGDP_PRJ)
G=0.461538/12 (Siberian)
A=0.475/19 (GENOME_DK)
HGVS:: NC_000010.11:g.88837102G>A, NC_000010.10:g.90596859G>A

Select item 121455512.

rs1214555 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 10:88837177 (GRCh38)
10:90596934 (GRCh37)
Canonical SPDI:: NC_000010.11:88837176:C:A,NC_000010.11:88837176:C:T
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.266373/3262 (ALFA)
T=0.212264/45 (Vietnamese)
T=0.324074/70 (Qatari)
T=0.331663/331 (GoNL)
T=0.336519/986 (KOREAN)
T=0.337887/5663 (TOMMO)
T=0.340076/1261 (TWINSUK)
T=0.349507/1347 (ALSPAC)
T=0.362991/665 (Korea1K)
T=0.37/222 (NorthernSweden)
C=0.38141/119 (SGDP_PRJ)
T=0.395536/1772 (Estonian)
T=0.404591/2026 (1000Genomes)
T=0.411319/108872 (TOPMED)
T=0.416667/135 (HapMap)
T=0.423318/59223 (GnomAD)
C=0.461538/12 (Siberian)
T=0.475/19 (GENOME_DK)
HGVS:: NC_000010.11:g.88837177C>A, NC_000010.11:g.88837177C>T, NC_000010.10:g.90596934C>A, NC_000010.10:g.90596934C>T

Select item 121455613.

rs1214556 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 10:88838290 (GRCh38)
10:90598047 (GRCh37)
Canonical SPDI:: NC_000010.11:88838289:G:C
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.4045/7641 (ALFA)
C=0.216981/46 (Vietnamese)
C=0.324074/70 (Qatari)
C=0.332665/332 (GoNL)
C=0.336519/986 (KOREAN)
C=0.33778/5661 (TOMMO)
C=0.340345/1262 (TWINSUK)
C=0.350285/1350 (ALSPAC)
C=0.363537/666 (Korea1K)
G=0.378205/118 (SGDP_PRJ)
C=0.388333/233 (NorthernSweden)
C=0.403342/2020 (1000Genomes)
C=0.411292/108865 (TOPMED)
C=0.412723/1849 (Estonian)
C=0.423894/59318 (GnomAD)
C=0.439024/144 (HapMap)
G=0.464286/13 (Siberian)
C=0.475/19 (GENOME_DK)
HGVS:: NC_000010.11:g.88838290G>C, NC_000010.10:g.90598047G>C

Select item 121455714.

rs1214557 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 10:88840383 (GRCh38)
10:90600140 (GRCh37)
Canonical SPDI:: NC_000010.11:88840382:G:A,NC_000010.11:88840382:G:T
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.27301/3340 (ALFA)
A=0.214286/45 (Vietnamese)
A=0.324074/70 (Qatari)
A=0.332665/332 (GoNL)
A=0.336177/985 (KOREAN)
A=0.337851/5662 (TOMMO)
A=0.340615/1263 (TWINSUK)
A=0.349766/1348 (ALSPAC)
A=0.363537/666 (Korea1K)
G=0.383871/119 (SGDP_PRJ)
A=0.388333/233 (NorthernSweden)
A=0.403029/2018 (1000Genomes)
A=0.411164/108831 (TOPMED)
A=0.412946/1850 (Estonian)
A=0.424056/59378 (GnomAD)
G=0.464286/13 (Siberian)
A=0.475/19 (GENOME_DK)
HGVS:: NC_000010.11:g.88840383G>A, NC_000010.11:g.88840383G>T, NC_000010.10:g.90600140G>A, NC_000010.10:g.90600140G>T

Select item 121455815.

rs1214558 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:88841108 (GRCh38)
10:90600865 (GRCh37)
Canonical SPDI:: NC_000010.11:88841107:A:G
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.34948/21637 (ALFA)
G=0.09434/20 (Vietnamese)
G=0.15802/463 (KOREAN)
G=0.16321/299 (Korea1K)
G=0.190476/16 (PRJEB36033)
G=0.210064/3521 (TOMMO)
G=0.268519/58 (Qatari)
G=0.275796/572 (HGDP_Stanford)
G=0.326653/326 (GoNL)
G=0.326983/1638 (1000Genomes)
G=0.334142/1239 (TWINSUK)
G=0.34302/1322 (ALSPAC)
G=0.361068/95571 (TOPMED)
G=0.361376/683 (HapMap)
G=0.378207/52896 (GnomAD)
G=0.385/231 (NorthernSweden)
G=0.405134/1815 (Estonian)
A=0.40873/103 (SGDP_PRJ)
A=0.464286/13 (Siberian)
G=0.475/19 (GENOME_DK)
HGVS:: NC_000010.11:g.88841108A>G, NC_000010.10:g.90600865A>G

Select item 121455916.

rs1214559 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:88841553 (GRCh38)
10:90601310 (GRCh37)
Canonical SPDI:: NC_000010.11:88841552:T:C
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.383005/11818 (ALFA)
C=0.199074/43 (Vietnamese)
C=0.324074/70 (Qatari)
C=0.332665/332 (GoNL)
C=0.336519/986 (KOREAN)
C=0.337745/5661 (TOMMO)
C=0.340615/1263 (TWINSUK)
C=0.349248/1346 (ALSPAC)
C=0.364083/667 (Korea1K)
T=0.380645/118 (SGDP_PRJ)
C=0.388333/233 (NorthernSweden)
C=0.401312/2010 (1000Genomes)
C=0.41116/108830 (TOPMED)
C=0.412946/1850 (Estonian)
C=0.424066/59292 (GnomAD)
T=0.464286/13 (Siberian)
C=0.469697/124 (HapMap)
C=0.475/19 (GENOME_DK)
HGVS:: NC_000010.11:g.88841553T>C, NC_000010.10:g.90601310T>C

Select item 121456017.

rs1214560 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 10:88841690 (GRCh38)
10:90601447 (GRCh37)
Canonical SPDI:: NC_000010.11:88841689:G:C,NC_000010.11:88841689:G:T
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.227782/3009 (ALFA)
C=0.042453/9 (Vietnamese)
C=0.057153/167 (KOREAN)
C=0.06714/123 (Korea1K)
C=0.105032/1760 (TOMMO)
C=0.236111/51 (Qatari)
C=0.251249/1258 (1000Genomes)
C=0.304904/80705 (TOPMED)
C=0.321643/321 (GoNL)
C=0.32536/45514 (GnomAD)
C=0.32767/1215 (TWINSUK)
C=0.335236/1292 (ALSPAC)
C=0.38/228 (NorthernSweden)
C=0.392188/1757 (Estonian)
G=0.445/89 (SGDP_PRJ)
C=0.45/18 (GENOME_DK)
G=0.461538/12 (Siberian)
HGVS:: NC_000010.11:g.88841690G>C, NC_000010.11:g.88841690G>T, NC_000010.10:g.90601447G>C, NC_000010.10:g.90601447G>T

Select item 121456118.

rs1214561 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:88842651 (GRCh38)
10:90602408 (GRCh37)
Canonical SPDI:: NC_000010.11:88842650:A:C
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.392324/7411 (ALFA)
C=0.157338/461 (KOREAN)
C=0.163755/300 (Korea1K)
C=0.210029/3520 (TOMMO)
C=0.291667/63 (Qatari)
C=0.325651/325 (GoNL)
C=0.333064/1235 (TWINSUK)
C=0.341723/1317 (ALSPAC)
C=0.356184/1784 (1000Genomes)
A=0.38189/97 (SGDP_PRJ)
C=0.385/231 (NorthernSweden)
C=0.390819/103446 (TOPMED)
C=0.404238/56409 (GnomAD)
C=0.404464/1812 (Estonian)
C=0.407407/132 (HapMap)
A=0.464286/13 (Siberian)
C=0.475/19 (GENOME_DK)
HGVS:: NC_000010.11:g.88842651A>C, NC_000010.10:g.90602408A>C

Select item 121456219.

rs1214562 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:88842660 (GRCh38)
10:90602417 (GRCh37)
Canonical SPDI:: NC_000010.11:88842659:A:C
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.404659/7644 (ALFA)
C=0.221698/47 (Vietnamese)
C=0.324074/70 (Qatari)
C=0.332665/332 (GoNL)
C=0.336177/985 (KOREAN)
C=0.337887/5663 (TOMMO)
C=0.339266/1258 (TWINSUK)
C=0.348729/1344 (ALSPAC)
C=0.353873/402 (Daghestan)
C=0.364083/667 (Korea1K)
A=0.378981/119 (SGDP_PRJ)
C=0.388333/233 (NorthernSweden)
C=0.403654/2021 (1000Genomes)
C=0.411607/1844 (Estonian)
C=0.412845/109276 (TOPMED)
C=0.423409/59058 (GnomAD)
A=0.464286/13 (Siberian)
C=0.475/19 (GENOME_DK)
A=0.487805/80 (HapMap)
HGVS:: NC_000010.11:g.88842660A>C, NC_000010.10:g.90602417A>C

Select item 121456320.

rs1214563 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:88842871 (GRCh38)
10:90602628 (GRCh37)
Canonical SPDI:: NC_000010.11:88842870:A:G
Gene:: ANKRD22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.36856/18013 (ALFA)
G=0.103774/22 (Vietnamese)
G=0.158703/465 (KOREAN)
G=0.163755/300 (Korea1K)
G=0.188498/118 (Chileans)
G=0.209994/3519 (TOMMO)
G=0.291667/63 (Qatari)
G=0.324649/324 (GoNL)
G=0.334951/1242 (TWINSUK)
G=0.34302/1322 (ALSPAC)
G=0.356496/1785 (1000Genomes)
A=0.38189/97 (SGDP_PRJ)
G=0.385/231 (NorthernSweden)
G=0.390801/103441 (TOPMED)
G=0.405357/1816 (Estonian)
G=0.406417/56861 (GnomAD)
G=0.410392/774 (HapMap)
A=0.464286/13 (Siberian)
G=0.475/19 (GENOME_DK)
HGVS:: NC_000010.11:g.88842871A>G, NC_000010.10:g.90602628A>G

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