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rs397515335

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515335(-;-)
Make rs397515335(-;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position243344278
GeneMIR4677, SDCCAG8
is asnp
is mentioned by
dbSNPrs397515335
ebirs397515335
HLIrs397515335
Exacrs397515335
Varsomers397515335
Maprs397515335
PheGenIrs397515335
hapmaprs397515335
1000 genomesrs397515335
hgdprs397515335
ensemblrs397515335
gopubmedrs397515335
geneviewrs397515335
scholarrs397515335
googlers397515335
pharmgkbrs397515335
gwascentralrs397515335
openSNPrs397515335
23andMers397515335
23andMe allrs397515335
SNP Nexus

SNPshotrs397515335
SNPdbers397515335
MSV3drs397515335
GWAS Ctlgrs397515335
Max Magnitude0
ClinVar
Risk rs397515335(;)
Alt rs397515335(;)
Reference rs397515335(G;G)
Significance Pathogenic
Disease Senior-Loken syndrome 7
Variation info
Gene SDCCAG8 MIR4677
CLNDBN Senior-Loken syndrome 7
Reversed 0
HGVS NC_000001.10:g.243507580delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000000074.4,