Original source

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

Alleles
A/G/T|Ancestral: A|Ambiguity code: D|MAF: 0.02 (T)
Location

Chromosome 17:63917608 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 14 transcripts, has 2522 sample genotypes and is mentioned in 1 citation.

Variant displays