Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K
Location

Chromosome 2:127423087 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CX067274

Most severe consequence
 
Missense variant
Synonyms

LSDB PC-HY12

HGVS names

This variant has 17 HGVS names - Show

About this variant

This variant overlaps 12 transcripts.

Variant displays