Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 2:118847749 (forward strand) | View in location tab

Most severe consequence
HGVS name

2:g.118847749T>G

About this variant

This variant overlaps 3 transcripts.

Variation displays