Original source

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

Alleles
C/G | Ambiguity code: S | MAF: 0.37 (C)
Location

Chromosome 19:44905910 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR033687

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs678339, rs11542028

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts, has 2510 individual genotypes and is mentioned in 27 citations.

Variation displays