Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.22 (A)
Location

Chromosome 3:49701983 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56540553, rs57210211

This variation has 2 HGVS names - click the plus to show

3:g.49701983G>A
ENST00000296452.4:c.11736G>A

This variation has assays on 8 chips - click the plus to show

Variation displays