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rs1001153999

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position50720446
GeneSHANK3
is asnp
is mentioned by
dbSNPrs1001153999
dbSNP (classic)rs1001153999
ClinGenrs1001153999
ebirs1001153999
HLIrs1001153999
Exacrs1001153999
Gnomadrs1001153999
Varsomers1001153999
LitVarrs1001153999
Maprs1001153999
PheGenIrs1001153999
Biobankrs1001153999
1000 genomesrs1001153999
hgdprs1001153999
ensemblrs1001153999
geneviewrs1001153999
scholarrs1001153999
googlers1001153999
pharmgkbrs1001153999
gwascentralrs1001153999
openSNPrs1001153999
23andMers1001153999
SNPshotrs1001153999
SNPdbers1001153999
MSV3drs1001153999
GWAS Ctlgrs1001153999
Max Magnitude0
ClinVar
Risk rs1001153999(T;T)
Alt rs1001153999(T;T)
Reference Rs1001153999(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SHANK3
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.51158874C>G
CLNSRC
CLNACC RCV000412919.1,