Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.16 (C)
Location

Chromosome 6:52419923 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3761989

HGVS name

6:g.52419923G>C

About this variant

This variant overlaps 5 transcripts and has 2509 individual genotypes.

Variation displays