Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.01 (C)
Location

Chromosome 1:186680587 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.186680587G>C

About this variant

This variant overlaps 7 transcripts, has 2915 individual genotypes and is mentioned in 4 citations.

Variation displays