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rs387907194

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907194(A;A)
Make rs387907194(A;G)
ReferenceGRCh37.p10 37.5/138
Chromosome9
Position2110356
GeneSMARCA2
is asnp
is mentioned by
dbSNPrs387907194
ebirs387907194
HLIrs387907194
Exacrs387907194
Varsomers387907194
Maprs387907194
PheGenIrs387907194
hapmaprs387907194
1000 genomesrs387907194
hgdprs387907194
ensemblrs387907194
gopubmedrs387907194
geneviewrs387907194
scholarrs387907194
googlers387907194
pharmgkbrs387907194
gwascentralrs387907194
openSNPrs387907194
23andMers387907194
23andMe allrs387907194
SNP Nexus

SNPshotrs387907194
SNPdbers387907194
MSV3drs387907194
GWAS Ctlgrs387907194
Max Magnitude0
ClinVar
Risk rs387907194(A;A)
Alt rs387907194(A;A)
Reference rs387907194(G;G)
Significance Pathogenic
Disease Nicolaides-Baraitser syndrome
Variation info
Gene SMARCA2
CLNDBN Nicolaides-Baraitser syndrome
Reversed 0
HGVS NC_000009.11:g.2110356G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000024365.5,