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rs797044856

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044856(C;C)
Make rs797044856(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11021968
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs797044856
ebirs797044856
HLIrs797044856
Exacrs797044856
Varsomers797044856
Maprs797044856
PheGenIrs797044856
hapmaprs797044856
1000 genomesrs797044856
hgdprs797044856
ensemblrs797044856
gopubmedrs797044856
geneviewrs797044856
scholarrs797044856
googlers797044856
pharmgkbrs797044856
gwascentralrs797044856
openSNPrs797044856
23andMers797044856
23andMe allrs797044856
SNP Nexus

SNPshotrs797044856
SNPdbers797044856
MSV3drs797044856
GWAS Ctlgrs797044856
Max Magnitude0
ClinVar
Risk rs797044856(C;C)
Alt rs797044856(C;C)
Reference rs797044856(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SMARCA4
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000019.9:g.11132644G>C
CLNSRC
CLNACC RCV000190658.1,