Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.07 (C)
Location

Chromosome 4:65341645 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2759 individual genotypes.

Variation displays