Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S
Location

Chromosome 17:7668975 (forward strand)|View in location tab

Co-located variant

dbSNP rs371242826 (CG/TC)

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs35756168

HGVS names

This variant has 36 HGVS names - Show

About this variant

This variant overlaps 37 transcripts.

Variant displays