Have questions? Visit https://www.reddit.com/r/SNPedia

rs398122826

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122826(C;T)
Make rs398122826(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position38245752
GeneDDHD2
is asnp
is mentioned by
dbSNPrs398122826
ebirs398122826
HLIrs398122826
Exacrs398122826
Varsomers398122826
Maprs398122826
PheGenIrs398122826
hapmaprs398122826
1000 genomesrs398122826
hgdprs398122826
ensemblrs398122826
gopubmedrs398122826
geneviewrs398122826
scholarrs398122826
googlers398122826
pharmgkbrs398122826
gwascentralrs398122826
openSNPrs398122826
23andMers398122826
23andMe allrs398122826
SNP Nexus

SNPshotrs398122826
SNPdbers398122826
MSV3drs398122826
GWAS Ctlgrs398122826
Max Magnitude0
ClinVar
Risk rs398122826(A,T;A,T)
Alt rs398122826(A,T;A,T)
Reference rs398122826(C;C)
Significance Pathogenic
Disease Spastic paraplegia 54
Variation info
Gene DDHD2
CLNDBN Spastic paraplegia 54, autosomal recessive
Reversed 0
HGVS NC_000008.10:g.38103270C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032885.5,