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Select item 109321.

rs10932 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 22:35194894 (GRCh38)
22:35590887 (GRCh37)
Canonical SPDI:: NC_000022.11:35194893:G:A,NC_000022.11:35194893:G:T
Gene:: LINC01399 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000022.11:g.35194894G>A, NC_000022.11:g.35194894G>T, NC_000022.10:g.35590887G>A, NC_000022.10:g.35590887G>T, NG_001300.3:g.234C>T, NG_001300.3:g.234C>A, NR_126356.1:n.185C>T, NR_126356.1:n.185C>A

Supplemental Content

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