Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 19:840713 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs597148

HGVS name

19:g.840713G>C

Variation displays