Original source

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

Alleles
T/G | Ambiguity code: K
Location

Chromosome 8:6981012 (forward strand) | View in location tab

Most severe consequence
Synonyms

Archive dbSNP rs141551840

HGVS name

8:g.6981012T>G

About this variant

This variant overlaps 2 transcripts and has 1 individual genotype.

Variation displays