Original source

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

Alleles
A/G/T/C | Ancestral: A | Ambiguity code: N
Location

Chromosome 17:41267762 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM040687, CM041683, CM087249

Most severe consequence
Clinical significance

Synonyms

LSDB U14680.1:c.115T>C, U14680.1:c.115T>A

This variation has 138 HGVS names - click the plus to show

Variation displays