Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

Chromosome 12:71938143 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR056785

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60080807

HGVS name

12:g.71938143G>T

This variation has assays on 6 chips - click the plus to show

Variation displays