Original source

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

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

Chromosome 17:47545158 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs2317805

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 2 sample genotypes.

Variant displays