Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.01 (T)
Location

Chromosome 18:31400451 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59606563, rs12967498

HGVS names

This variant has 6 HGVS names - Show

About this variant

Variant displays