Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D|MAF: 0.36 (G)
Location

Chromosome 4:3503136 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60912361

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2511 sample genotypes.

Variant displays