Original source

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

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

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