Original source

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

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

Chromosome 1:12165862 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17882725, rs36205947

HGVS name

1:g.12165862A>C

About this variant

This variant overlaps 4 transcripts, has 2629 individual genotypes and is mentioned in 1 citation.

Variation displays