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

rs387906275

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906275(-;-)
Make rs387906275(-;A)
Make rs387906275(A;A)
ReferenceGRCh38 38.1/141
Chromosome15
Position64969322
GeneSPG21
is asnp
is mentioned by
dbSNPrs387906275
ebirs387906275
HLIrs387906275
Exacrs387906275
Varsomers387906275
Maprs387906275
PheGenIrs387906275
hapmaprs387906275
1000 genomesrs387906275
hgdprs387906275
ensemblrs387906275
gopubmedrs387906275
geneviewrs387906275
scholarrs387906275
googlers387906275
pharmgkbrs387906275
gwascentralrs387906275
openSNPrs387906275
23andMers387906275
23andMe allrs387906275
SNP Nexus

SNPshotrs387906275
SNPdbers387906275
MSV3drs387906275
GWAS Ctlgrs387906275
Max Magnitude0
ClinVar
Risk rs387906275(A;A)
Alt rs387906275(A;A)
Reference rs387906275(;)
Significance Pathogenic
Disease Mast syndrome
Variation info
Gene SPG21
CLNDBN Mast syndrome
Reversed 1
HGVS NC_000015.9:g.65261660dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000002596.3,