SNP Links for Nucleotide (Select 374349243) - SNP

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Links from Nucleotide

Items: 1 to 20 of 366

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Select item 14893708001.

rs1489370800 has merged into rs3931273 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: NT_113793.3:162345 (GRCh38)
NT_113793.3:142697779 (GRCh37)
Canonical SPDI:: NT_113793.3:162344:C:T
Gene:: ANKRD20A12P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.0192/86 (ALFA)
HGVS:: NT_113793.3:g.162345C>T, NC_000001.10:g.142697779C>T, NR_046228.1:n.1386G>A

Select item 14884142192.

rs1488414219 [Homo sapiens]

Variant type:: SNV:
Alleles:: C>T
Chromosome:: no mapping
Canonical SPDI:

Select item 14875695753.

rs1487569575 [Homo sapiens]

Variant type:: SNV:
Alleles:: G>A
Chromosome:: no mapping
Canonical SPDI:

Select item 14875080734.

rs1487508073 [Homo sapiens]

Variant type:: SNV:
Alleles:: A>T
Chromosome:: no mapping
Canonical SPDI:

Select item 14863202165.

rs1486320216 [Homo sapiens]

Variant type:: SNV:
Alleles:: C>T
Chromosome:: no mapping
Canonical SPDI:

Select item 14770721286.

rs1477072128 [Homo sapiens]

Variant type:: SNV:
Alleles:: T>A
Chromosome:: no mapping
Canonical SPDI:

Select item 14756998747.

rs1475699874 [Homo sapiens]

Variant type:: SNV:
Alleles:: G>T
Chromosome:: no mapping
Canonical SPDI:

Select item 14751367948.

rs1475136794 [Homo sapiens]

Variant type:: SNV:
Alleles:: C>G
Chromosome:: no mapping
Canonical SPDI:

Select item 14727861329.

rs1472786132 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: NT_113793.3:177902 (GRCh38)
NT_113793.3:142713336 (GRCh37)
Canonical SPDI:: NT_113793.3:177901:C:A
Gene:: ANKRD20A12P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.0002/1 (ALFA)
HGVS:: NT_113793.3:g.177902C>A, NC_000001.10:g.142713336C>A, NR_046228.1:n.270G>T

Select item 147228083110.

rs1472280831 [Homo sapiens]

Variant type:: SNV:
Alleles:: C>G
Chromosome:: no mapping
Canonical SPDI:

Select item 146682068411.

rs1466820684 [Homo sapiens]

Variant type:: SNV:
Alleles:: C>T
Chromosome:: no mapping
Canonical SPDI:

Select item 146420308912.

rs1464203089 [Homo sapiens]

Variant type:: SNV:
Alleles:: C>A
Chromosome:: no mapping
Canonical SPDI:

Select item 146231286013.

rs1462312860 [Homo sapiens]

Variant type:: SNV:
Alleles:: T>C
Chromosome:: no mapping
Canonical SPDI:

Select item 146229030914.

rs1462290309 [Homo sapiens]

Variant type:: SNV:
Alleles:: T>C
Chromosome:: no mapping
Canonical SPDI:

Select item 146108599015.

rs1461085990 [Homo sapiens]

Variant type:: SNV:
Alleles:: G>A
Chromosome:: no mapping
Canonical SPDI:

Select item 146102571616.

rs1461025716 [Homo sapiens]

Variant type:: SNV:
Alleles:: T>G
Chromosome:: no mapping
Canonical SPDI:

Select item 145565469017.

rs1455654690 has merged into rs201799719 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: NT_113793.3:178112 (GRCh38)
NT_113793.3:142713546 (GRCh37)
Canonical SPDI:: NT_113793.3:178111:C:G
Gene:: ANKRD20A12P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.2969/1327 (ALFA)
HGVS:: NT_113793.3:g.178112C>G, NC_000001.10:g.142713546C>G, NR_046228.1:n.60G>C

Select item 145559437018.

rs1455594370 [Homo sapiens]

Variant type:: SNV:
Alleles:: C>T
Chromosome:: no mapping
Canonical SPDI:

Select item 145507213419.

rs1455072134 [Homo sapiens]

Variant type:: SNV:
Alleles:: A>G
Chromosome:: no mapping
Canonical SPDI:

Select item 145497962020.

rs1454979620 [Homo sapiens]

Variant type:: SNV:
Alleles:: A>G
Chromosome:: no mapping
Canonical SPDI:

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