SNP Links for Nucleotide (Select 223555930) - SNP - NCBI

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Links from Nucleotide

Items: 3

Select item 169946391.

rs16994639 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:34771 (GRCh38)
1:34771 (GRCh37)
Canonical SPDI:: NC_000001.11:34770:G:C
Gene:: FAM138A (Varview), MIR1302-2HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000001.11:g.34771G>C, NC_000001.10:g.34771G>C, XR_007065314.1:n.1616G>C, NR_026818.1:n.970C>G

Select item 112668622.

rs11266862 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:34810 (GRCh38)
1:34810 (GRCh37)
Canonical SPDI:: NC_000001.11:34809:A:T
Gene:: FAM138A (Varview), MIR1302-2HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000001.11:g.34810A>T, NC_000001.10:g.34810A>T, XR_007065314.1:n.1655A>T, NR_026818.1:n.931T>A

Select item 38717343.

rs3871734 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:35082 (GRCh38)
1:35082 (GRCh37)
Canonical SPDI:: NC_000001.11:35081:G:A
Gene:: FAM138A (Varview), MIR1302-2HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000001.11:g.35082G>A, NC_000001.10:g.35082G>A, XR_007065314.1:n.1927G>A, NR_026818.1:n.659C>T

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