Original source

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

Alleles
T/G | Ambiguity code: K
Location

Chromosome 6:111606615 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58747618

HGVS name

6:g.111606615T>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 7 transcripts.

Variation displays