Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.20 (T)
Location

Chromosome 19:44905307 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR982406

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs665261, rs1081104

HGVS name

19:g.44905307A>T

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 12 transcripts, has 2505 individual genotypes and is mentioned in 14 citations.

Variation displays