Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.44 (A)
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs63170661

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

About this variant

This variant overlaps 3 transcripts, has 2510 sample genotypes and is mentioned in 1 citation.

Variant displays