Original source

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

Alleles
T/A/C/G | Ancestral: T | Ambiguity code: N | MAF: 0.12 (C)
Location

Chromosome 15:75012985 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM940327

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

This variation has 27 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

Variation displays