Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

Chromosome 6:34426901 (forward strand) | View in location tab

Most severe consequence
HGVS name

6:g.34426901T>G

Variation displays