Original source

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

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

Chromosome 6:10397883 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and is mentioned in 4 citations.

Variant displays