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 17:50201450 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM062525

Most severe consequence
 
Missense variant
Synonyms

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and 2 regulatory features.

Variant displays