Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: < 0.01 (A)
Location

Chromosome 17:63917657 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs77064472

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2505 sample genotypes.

Variant displays