SNP Links for Nucleotide (Select 1032528833) - SNP

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:122105506 (GRCh38)
11:121976214 (GRCh37)
Canonical SPDI:: NC_000011.10:122105505:A:G
Gene:: MIR100HG (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.122105506A>G, NC_000011.9:g.121976214A>G, NR_137196.1:n.111T>C, NR_137195.1:n.111T>C

Select item 14859852088.

rs1485985208 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:122105485 (GRCh38)
11:121976193 (GRCh37)
Canonical SPDI:: NC_000011.10:122105484:G:A
Gene:: MIR100HG (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
HGVS:: NC_000011.10:g.122105485G>A, NC_000011.9:g.121976193G>A, NR_137196.1:n.132C>T, NR_137195.1:n.132C>T

Select item 14850777269.

rs1485077726 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:122090366 (GRCh38)
11:121961074 (GRCh37)
Canonical SPDI:: NC_000011.10:122090365:A:G,NC_000011.10:122090365:A:T
Gene:: MIR100HG (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00022/1 (ALFA)
G=0.00004/1 (TOMMO)
T=0.00022/1 (Estonian)
HGVS:: NC_000011.10:g.122090366A>G, NC_000011.10:g.122090366A>T, NC_000011.9:g.121961074A>G, NC_000011.9:g.121961074A>T, NR_024430.2:n.1866T>C, NR_024430.2:n.1866T>A, NR_024430.1:n.1819T>C, NR_024430.1:n.1819T>A, NR_137190.1:n.2191T>C, NR_137190.1:n.2191T>A, NR_137191.1:n.2170T>C, NR_137191.1:n.2170T>A, NR_137189.1:n.2158T>C, NR_137189.1:n.2158T>A, NR_137175.1:n.2137T>C, NR_137175.1:n.2137T>A, NR_137192.1:n.2030T>C, NR_137192.1:n.2030T>A, NR_137196.1:n.1921T>C, NR_137196.1:n.1921T>A, NR_137195.1:n.1900T>C, NR_137195.1:n.1900T>A, NR_137180.1:n.1878T>C, NR_137180.1:n.1878T>A, NR_137193.1:n.1857T>C, NR_137193.1:n.1857T>A, NR_137176.1:n.1848T>C, NR_137176.1:n.1848T>A, NR_137182.1:n.1845T>C, NR_137182.1:n.1845T>A, NR_137177.1:n.1827T>C, NR_137177.1:n.1827T>A, NR_137179.1:n.1820T>C, NR_137179.1:n.1820T>A, NR_137181.1:n.1763T>C, NR_137181.1:n.1763T>A, NR_137183.1:n.1754T>C, NR_137183.1:n.1754T>A, NR_137185.1:n.1733T>C, NR_137185.1:n.1733T>A, NR_137194.1:n.1732T>C, NR_137194.1:n.1732T>A, NR_137188.1:n.1711T>C, NR_137188.1:n.1711T>A, NR_137184.1:n.1672T>C, NR_137184.1:n.1672T>A, NR_137186.1:n.1642T>C, NR_137186.1:n.1642T>A, NR_137187.1:n.1621T>C, NR_137187.1:n.1621T>A

Select item 148394574210.

rs1483945742 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:122090323 (GRCh38)
11:121961031 (GRCh37)
Canonical SPDI:: NC_000011.10:122090322:T:C
Gene:: MIR100HG (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.122090323T>C, NC_000011.9:g.121961031T>C, NR_024430.2:n.1909A>G, NR_024430.1:n.1862A>G, NR_137190.1:n.2234A>G, NR_137191.1:n.2213A>G, NR_137189.1:n.2201A>G, NR_137175.1:n.2180A>G, NR_137192.1:n.2073A>G, NR_137196.1:n.1964A>G, NR_137195.1:n.1943A>G, NR_137180.1:n.1921A>G, NR_137193.1:n.1900A>G, NR_137176.1:n.1891A>G, NR_137182.1:n.1888A>G, NR_137177.1:n.1870A>G, NR_137179.1:n.1863A>G, NR_137181.1:n.1806A>G, NR_137183.1:n.1797A>G, NR_137185.1:n.1776A>G, NR_137194.1:n.1775A>G, NR_137188.1:n.1754A>G, NR_137184.1:n.1715A>G, NR_137186.1:n.1685A>G, NR_137187.1:n.1664A>G

Select item 148230929211.

rs1482309292 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:122105552 (GRCh38)
11:121976260 (GRCh37)
Canonical SPDI:: NC_000011.10:122105551:A:G
Gene:: MIR100HG (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.122105552A>G, NC_000011.9:g.121976260A>G, NR_137196.1:n.65T>C, NR_137195.1:n.65T>C

Select item 148197695412.

rs1481976954 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:122089424 (GRCh38)
11:121960132 (GRCh37)
Canonical SPDI:: NC_000011.10:122089423:T:C
Gene:: MIR100HG (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.122089424T>C, NC_000011.9:g.121960132T>C, NR_024430.2:n.2808A>G, NR_024430.1:n.2761A>G, NR_137190.1:n.3133A>G, NR_137191.1:n.3112A>G, NR_137189.1:n.3100A>G, NR_137175.1:n.3079A>G, NR_137192.1:n.2972A>G, NR_137196.1:n.2863A>G, NR_137195.1:n.2842A>G, NR_137180.1:n.2820A>G, NR_137193.1:n.2799A>G, NR_137176.1:n.2790A>G, NR_137182.1:n.2787A>G, NR_137177.1:n.2769A>G, NR_137179.1:n.2762A>G, NR_137181.1:n.2705A>G, NR_137183.1:n.2696A>G, NR_137185.1:n.2675A>G, NR_137194.1:n.2674A>G, NR_137188.1:n.2653A>G, NR_137184.1:n.2614A>G, NR_137186.1:n.2584A>G, NR_137187.1:n.2563A>G

Select item 148129632213.

rs1481296322 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:122091548 (GRCh38)
11:121962256 (GRCh37)
Canonical SPDI:: NC_000011.10:122091547:G:A
Gene:: MIR100HG (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.122091548G>A, NC_000011.9:g.121962256G>A, NR_024430.2:n.684C>T, NR_024430.1:n.637C>T, NR_137190.1:n.1009C>T, NR_137191.1:n.988C>T, NR_137189.1:n.976C>T, NR_137175.1:n.955C>T, NR_137192.1:n.848C>T, NR_137196.1:n.739C>T, NR_137195.1:n.718C>T, NR_137180.1:n.696C>T, NR_137193.1:n.675C>T, NR_137176.1:n.666C>T, NR_137182.1:n.663C>T, NR_137177.1:n.645C>T, NR_137179.1:n.638C>T, NR_137181.1:n.581C>T, NR_137183.1:n.572C>T, NR_137185.1:n.551C>T, NR_137194.1:n.550C>T, NR_137188.1:n.529C>T, NR_137184.1:n.490C>T, NR_137186.1:n.460C>T, NR_137187.1:n.439C>T

Select item 148079232414.

rs1480792324 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:122090723 (GRCh38)
11:121961431 (GRCh37)
Canonical SPDI:: NC_000011.10:122090722:T:A,NC_000011.10:122090722:T:C
Gene:: MIR100HG (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.122090723T>A, NC_000011.10:g.122090723T>C, NC_000011.9:g.121961431T>A, NC_000011.9:g.121961431T>C, NR_024430.2:n.1509A>T, NR_024430.2:n.1509A>G, NR_024430.1:n.1462A>T, NR_024430.1:n.1462A>G, NR_137190.1:n.1834A>T, NR_137190.1:n.1834A>G, NR_137191.1:n.1813A>T, NR_137191.1:n.1813A>G, NR_137189.1:n.1801A>T, NR_137189.1:n.1801A>G, NR_137175.1:n.1780A>T, NR_137175.1:n.1780A>G, NR_137192.1:n.1673A>T, NR_137192.1:n.1673A>G, NR_137196.1:n.1564A>T, NR_137196.1:n.1564A>G, NR_137195.1:n.1543A>T, NR_137195.1:n.1543A>G, NR_137180.1:n.1521A>T, NR_137180.1:n.1521A>G, NR_137193.1:n.1500A>T, NR_137193.1:n.1500A>G, NR_137176.1:n.1491A>T, NR_137176.1:n.1491A>G, NR_137182.1:n.1488A>T, NR_137182.1:n.1488A>G, NR_137177.1:n.1470A>T, NR_137177.1:n.1470A>G, NR_137179.1:n.1463A>T, NR_137179.1:n.1463A>G, NR_137181.1:n.1406A>T, NR_137181.1:n.1406A>G, NR_137183.1:n.1397A>T, NR_137183.1:n.1397A>G, NR_137185.1:n.1376A>T, NR_137185.1:n.1376A>G, NR_137194.1:n.1375A>T, NR_137194.1:n.1375A>G, NR_137188.1:n.1354A>T, NR_137188.1:n.1354A>G, NR_137184.1:n.1315A>T, NR_137184.1:n.1315A>G, NR_137186.1:n.1285A>T, NR_137186.1:n.1285A>G, NR_137187.1:n.1264A>T, NR_137187.1:n.1264A>G

Select item 147971784115.

rs1479717841 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:122105241 (GRCh38)
11:121975949 (GRCh37)
Canonical SPDI:: NC_000011.10:122105240:G:A
Gene:: MIR100HG (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.122105241G>A, NC_000011.9:g.121975949G>A, NR_137196.1:n.376C>T, NR_137195.1:n.376C>T

Select item 147941011116.

rs1479410111 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:122091721 (GRCh38)
11:121962429 (GRCh37)
Canonical SPDI:: NC_000011.10:122091720:T:C
Gene:: MIR100HG (Varview)
Functional Consequence:: intron_variant,splice_acceptor_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.122091721T>C, NC_000011.9:g.121962429T>C, NR_024430.2:n.511A>G, NR_024430.1:n.464A>G, NR_137190.1:n.836A>G, NR_137189.1:n.803A>G, NR_137196.1:n.566A>G, NR_137180.1:n.523A>G, NR_137176.1:n.493A>G, NR_137179.1:n.465A>G, NR_137183.1:n.399A>G, NR_137194.1:n.377A>G, NR_137184.1:n.317A>G, NR_137186.1:n.287A>G

Select item 147926688817.

rs1479266888 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:122089924 (GRCh38)
11:121960632 (GRCh37)
Canonical SPDI:: NC_000011.10:122089923:T:C
Gene:: MIR100HG (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.00003/8 (TOPMED)
HGVS:: NC_000011.10:g.122089924T>C, NC_000011.9:g.121960632T>C, NR_024430.2:n.2308A>G, NR_024430.1:n.2261A>G, NR_137190.1:n.2633A>G, NR_137191.1:n.2612A>G, NR_137189.1:n.2600A>G, NR_137175.1:n.2579A>G, NR_137192.1:n.2472A>G, NR_137196.1:n.2363A>G, NR_137195.1:n.2342A>G, NR_137180.1:n.2320A>G, NR_137193.1:n.2299A>G, NR_137176.1:n.2290A>G, NR_137182.1:n.2287A>G, NR_137177.1:n.2269A>G, NR_137179.1:n.2262A>G, NR_137181.1:n.2205A>G, NR_137183.1:n.2196A>G, NR_137185.1:n.2175A>G, NR_137194.1:n.2174A>G, NR_137188.1:n.2153A>G, NR_137184.1:n.2114A>G, NR_137186.1:n.2084A>G, NR_137187.1:n.2063A>G

Select item 147882386218.

rs1478823862 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:122090908 (GRCh38)
11:121961616 (GRCh37)
Canonical SPDI:: NC_000011.10:122090907:C:A,NC_000011.10:122090907:C:T
Gene:: MIR100HG (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.122090908C>A, NC_000011.10:g.122090908C>T, NC_000011.9:g.121961616C>A, NC_000011.9:g.121961616C>T, NR_024430.2:n.1324G>T, NR_024430.2:n.1324G>A, NR_024430.1:n.1277G>T, NR_024430.1:n.1277G>A, NR_137190.1:n.1649G>T, NR_137190.1:n.1649G>A, NR_137191.1:n.1628G>T, NR_137191.1:n.1628G>A, NR_137189.1:n.1616G>T, NR_137189.1:n.1616G>A, NR_137175.1:n.1595G>T, NR_137175.1:n.1595G>A, NR_137192.1:n.1488G>T, NR_137192.1:n.1488G>A, NR_137196.1:n.1379G>T, NR_137196.1:n.1379G>A, NR_137195.1:n.1358G>T, NR_137195.1:n.1358G>A, NR_137180.1:n.1336G>T, NR_137180.1:n.1336G>A, NR_137193.1:n.1315G>T, NR_137193.1:n.1315G>A, NR_137176.1:n.1306G>T, NR_137176.1:n.1306G>A, NR_137182.1:n.1303G>T, NR_137182.1:n.1303G>A, NR_137177.1:n.1285G>T, NR_137177.1:n.1285G>A, NR_137179.1:n.1278G>T, NR_137179.1:n.1278G>A, NR_137181.1:n.1221G>T, NR_137181.1:n.1221G>A, NR_137183.1:n.1212G>T, NR_137183.1:n.1212G>A, NR_137185.1:n.1191G>T, NR_137185.1:n.1191G>A, NR_137194.1:n.1190G>T, NR_137194.1:n.1190G>A, NR_137188.1:n.1169G>T, NR_137188.1:n.1169G>A, NR_137184.1:n.1130G>T, NR_137184.1:n.1130G>A, NR_137186.1:n.1100G>T, NR_137186.1:n.1100G>A, NR_137187.1:n.1079G>T, NR_137187.1:n.1079G>A

Select item 147677628219.

rs1476776282 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:122089260 (GRCh38)
11:121959968 (GRCh37)
Canonical SPDI:: NC_000011.10:122089259:T:G
Gene:: MIR100HG (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000015/4 (TOPMED)
G=0.000684/2 (KOREAN)
HGVS:: NC_000011.10:g.122089260T>G, NC_000011.9:g.121959968T>G, NR_024430.2:n.2972A>C, NR_024430.1:n.2925A>C, NR_137190.1:n.3297A>C, NR_137191.1:n.3276A>C, NR_137189.1:n.3264A>C, NR_137175.1:n.3243A>C, NR_137192.1:n.3136A>C, NR_137196.1:n.3027A>C, NR_137195.1:n.3006A>C, NR_137180.1:n.2984A>C, NR_137193.1:n.2963A>C, NR_137176.1:n.2954A>C, NR_137182.1:n.2951A>C, NR_137177.1:n.2933A>C, NR_137179.1:n.2926A>C, NR_137181.1:n.2869A>C, NR_137183.1:n.2860A>C, NR_137185.1:n.2839A>C, NR_137194.1:n.2838A>C, NR_137188.1:n.2817A>C, NR_137184.1:n.2778A>C, NR_137186.1:n.2748A>C, NR_137187.1:n.2727A>C

Select item 147548510020.

rs1475485100 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:122090786 (GRCh38)
11:121961494 (GRCh37)
Canonical SPDI:: NC_000011.10:122090785:T:C
Gene:: MIR100HG (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000011.10:g.122090786T>C, NC_000011.9:g.121961494T>C, NR_024430.2:n.1446A>G, NR_024430.1:n.1399A>G, NR_137190.1:n.1771A>G, NR_137191.1:n.1750A>G, NR_137189.1:n.1738A>G, NR_137175.1:n.1717A>G, NR_137192.1:n.1610A>G, NR_137196.1:n.1501A>G, NR_137195.1:n.1480A>G, NR_137180.1:n.1458A>G, NR_137193.1:n.1437A>G, NR_137176.1:n.1428A>G, NR_137182.1:n.1425A>G, NR_137177.1:n.1407A>G, NR_137179.1:n.1400A>G, NR_137181.1:n.1343A>G, NR_137183.1:n.1334A>G, NR_137185.1:n.1313A>G, NR_137194.1:n.1312A>G, NR_137188.1:n.1291A>G, NR_137184.1:n.1252A>G, NR_137186.1:n.1222A>G, NR_137187.1:n.1201A>G

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Result Filters

Validation Status

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Items: 1 to 20 of 636

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