Original source

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

G/A | Ancestral: C | Ambiguity code: R

Chromosome 5:150120233 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs62618696

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 1 sample genotype.

Variant displays