Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 6:1608453 (forward strand) | View in location tab

Most severe consequence
HGVS name

6:g.1608453T>G

About this variant

This variant overlaps 2 transcripts.

Variation displays