Original source

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

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

Chromosome 17:34357972 (forward strand) | View in location tab

Co-located

with dbSNP rs371384728 (G/-/A)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs63170661

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 1112 individual genotypes and is mentioned in 1 citation.

Variation displays