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rs869312933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GATTCCAGGTGG;GATTCCAGGTGG) 0 common in clinvar
(GGTGGATTCCA;GGTGGATTCCA) 0 common in clinvar
Make rs869312933(-;-)
Make rs869312933(-;ATTCCAGGTGG)
Make rs869312933(ATTCCAGGTGG;ATTCCAGGTGG)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position228351314
GeneOBSCN
is asnp
is mentioned by
dbSNPrs869312933
dbSNP (old)rs869312933
ClinGenrs869312933
ebirs869312933
HLIrs869312933
Exacrs869312933
Gnomadrs869312933
Varsomers869312933
Maprs869312933
PheGenIrs869312933
Biobankrs869312933
1000 genomesrs869312933
hgdprs869312933
ensemblrs869312933
gopubmedrs869312933
geneviewrs869312933
scholarrs869312933
googlers869312933
pharmgkbrs869312933
gwascentralrs869312933
openSNPrs869312933
23andMers869312933
23andMe allrs869312933
SNP Nexus

SNPshotrs869312933
SNPdbers869312933
MSV3drs869312933
GWAS Ctlgrs869312933
Max Magnitude0
ClinVar
Risk rs869312933(-;-)
Alt rs869312933(-;-)
Reference Rs869312933(GGTGGATTCCA;GGTGGATTCCA)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene OBSCN
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.228539015_228539025delATTCCAGGTGG
CLNSRC
CLNACC RCV000210654.1,