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rs387906218

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs387906218(-;G)
Make rs387906218(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position243341156
GeneSDCCAG8
is asnp
is mentioned by
dbSNPrs387906218
dbSNP (classic)rs387906218
ClinGenrs387906218
ebirs387906218
HLIrs387906218
Exacrs387906218
Gnomadrs387906218
Varsomers387906218
LitVarrs387906218
Maprs387906218
PheGenIrs387906218
Biobankrs387906218
1000 genomesrs387906218
hgdprs387906218
ensemblrs387906218
geneviewrs387906218
scholarrs387906218
googlers387906218
pharmgkbrs387906218
gwascentralrs387906218
openSNPrs387906218
23andMers387906218
SNPshotrs387906218
SNPdbers387906218
MSV3drs387906218
GWAS Ctlgrs387906218
Max Magnitude0
ClinVar
Risk rs387906218(G;G)
Alt rs387906218(G;G)
Reference Rs387906218(-;-)
Significance Pathogenic
Disease Senior-Loken syndrome 7
Variation info
Gene SDCCAG8
CLNDBN Senior-Loken syndrome 7
Reversed 0
HGVS NC_000001.10:g.243504458dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000000075.5,