Original source

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

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

Chromosome 1:91698441 (forward strand)|View in location tab

Co-located variant

dbSNP rs202030205 (C/-)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs71650462, rs57829068

HGVS names

This variant has 8 HGVS names - Show

About this variant

Variant displays