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rs863224922

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224922(G;T)
Make rs863224922(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position2060894
GeneSMARCA2
is asnp
is mentioned by
dbSNPrs863224922
ebirs863224922
HLIrs863224922
Exacrs863224922
Varsomers863224922
Maprs863224922
PheGenIrs863224922
hapmaprs863224922
1000 genomesrs863224922
hgdprs863224922
ensemblrs863224922
gopubmedrs863224922
geneviewrs863224922
scholarrs863224922
googlers863224922
pharmgkbrs863224922
gwascentralrs863224922
openSNPrs863224922
23andMers863224922
23andMe allrs863224922
SNP Nexus

SNPshotrs863224922
SNPdbers863224922
MSV3drs863224922
GWAS Ctlgrs863224922
Max Magnitude0
ClinVar
Risk rs863224922(T;T)
Alt rs863224922(T;T)
Reference rs863224922(G;G)
Significance Probable-Pathogenic
Disease Nicolaides-Baraitser syndrome
Variation info
Gene SMARCA2
CLNDBN Nicolaides-Baraitser syndrome
Reversed 0
HGVS NC_000009.11:g.2060894G>T
CLNSRC
CLNACC RCV000196887.1,