Original source

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

C/A|Ancestral: C|Ambiguity code: M|MAF: 0.09 (A)

Chromosome 1:12204814 (forward strand)|View in location tab

Co-located variant

dbSNP rs375304935 (C/ACAA)

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs58707651, rs9430687

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2506 sample genotypes.

Variant displays