Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.01 (G)
Location

Chromosome 17:63918814 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2505 sample genotypes and is mentioned in 1 citation.

Variant displays