Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

C/G|Ambiguity code: S

Chromosome 12:52289361 (forward strand)|View in location tab

Co-located variant

dbSNP rs539058207 (C/G)

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs12578637

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 6 sample genotypes.

Variant displays