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 4:849256 (forward strand) | View in location tab

Most severe consequence
HGVS name

4:g.849256T>G

About this variant

This variant overlaps 11 transcripts.

Variation displays