Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 7:155464862 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
HGVS name

7:g.155464862C>A

About this variant

This variant overlaps 1 transcript.

Variant displays