Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 5:171391965 (forward strand) | View in location tab


with dbSNP rs200103231 (A/-/G/GG/GGG)

Most severe consequence
Evidence status

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 1100 individual genotypes.

Variation displays