Original source

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

Alleles
A/C|Ancestral: C|Ambiguity code: M|MAF: 0.15 (C)
Location

Chromosome 1:156117073 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1200934

HGVS names

This variant has 13 HGVS names - Show

About this variant

Variant displays