Original source

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

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs62618696

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 1 individual genotype.

Variation displays