Have questions? Visit https://www.reddit.com/r/SNPedia

rs869312964

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312964(C;C)
Make rs869312964(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11013022
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs869312964
ebirs869312964
HLIrs869312964
Exacrs869312964
Varsomers869312964
Maprs869312964
PheGenIrs869312964
hapmaprs869312964
1000 genomesrs869312964
hgdprs869312964
ensemblrs869312964
gopubmedrs869312964
geneviewrs869312964
scholarrs869312964
googlers869312964
pharmgkbrs869312964
gwascentralrs869312964
openSNPrs869312964
23andMers869312964
23andMe allrs869312964
SNP Nexus

SNPshotrs869312964
SNPdbers869312964
MSV3drs869312964
GWAS Ctlgrs869312964
Max Magnitude0
ClinVar
Risk rs869312964(C;C)
Alt rs869312964(C;C)
Reference rs869312964(T;T)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SMARCA4
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000019.9:g.11123698T>C
CLNSRC
CLNACC RCV000210700.1,