Original source

Variants (including SNPs and indels) imported from dbSNP (release 139) | [View in dbSNP]

Alleles
A/C | Ambiguity code: M
Location

Ultracontig Ultra103:375699 (forward strand) | View in location tab

Most severe consequence
Synonyms

Ensembl ENSOANSNP1147557

This variation has 3 HGVS names - click the plus to show

Variation displays