Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: < 0.01 (A)
Location

Chromosome 22:19148546 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.19148546C>A

About this variant

This variant overlaps 5 transcripts and has 2504 individual genotypes.

Variation displays