Original source

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

Alleles
C/A | Ambiguity code: M | MAF: 0.39 (A)
Location

Chromosome 12:6379948 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57736204

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 21 transcripts and has 2505 individual genotypes.

Variation displays