Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 17:7668975 (forward strand) | View in location tab

Co-located

with dbSNP rs371242826 (CG/TC)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs35756168

This variation has 35 HGVS names - click the plus to show

Variation displays