Original source

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

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

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

Most severe consequence
HGVS name

7:g.155464862C>A

About this variant

This variant overlaps 1 transcript.

Variation displays