Original source

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

Alleles
T/A | Ambiguity code: W
Location

Chromosome 1:114737035 (forward strand) | View in location tab

Most severe consequence
Synonyms

ENSEMBL:celera ENSRNOSNP11773

HGVS name

1:g.114737035T>A

Variation displays