Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.36 (C)
Location

Chromosome 17:61996204 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR031006 ; dbSNP rs41318506 (C/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58303360

HGVS name

17:g.61996204T>C

Variation displays