Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.46 (G)
Location

Chromosome 17:43122889 (forward strand) | View in location tab

Co-located

with dbSNP rs199839105 (G/-)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1180358, rs8176084

This variant has 24 HGVS names - click the plus to show

About this variant

This variant overlaps 26 transcripts and has 2608 sample genotypes.

Variant displays