Original source

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

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

Chromosome 6:52419101 (forward strand) | View in location tab

Most severe consequence
HGVS name

6:g.52419101A>C

About this variant

This variant overlaps 4 transcripts and has 1 individual genotype.

Variation displays