Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 6:18122762 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM033787

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

6:g.18122762A>T
ENST00000340650.3:c.76T>A
ENSP00000345464.3:p.Cys26Ser

Variation displays