Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.38 (G)
Location

Chromosome 4:41746494 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3805359

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, has 2508 sample genotypes and is mentioned in 1 citation.

Variant displays