Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.32 (T)
Location

Chromosome 18:6941663 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61692496

HGVS name

18:g.6941663G>T

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 3972 individual genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variation displays