Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: < 0.01 (G)

Chromosome 3:136922808 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57933550

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2511 sample genotypes.

Variant displays