Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.25 (C)
Location

Chromosome 3:128484618 (forward strand) | View in location tab

Co-located

with dbSNP rs78134532 (-/TTTT)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60757577, rs66813696

This variation has 6 HGVS names - click the plus to show

Variation displays