Original source

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

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

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

Co-located

with dbSNP rs371242826 (CG/TC)

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs35756168

This variant has 35 HGVS names - click the plus to show

About this variant

This variant overlaps 36 transcripts.

Variant displays