Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.01 (T)
Location

Chromosome 4:3487449 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61391692

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2506 sample genotypes.

Variant displays