Original source

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

Alleles
G/C|Ambiguity code: S
Location

Chromosome 1:120488733 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

1:g.120488733G>C

About this variant

This variant overlaps 1 transcript.

Variant displays