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rs786205472

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205472(C;C)
Make rs786205472(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position119345487
GeneC1QTNF5, MFRP
is asnp
is mentioned by
dbSNPrs786205472
ebirs786205472
HLIrs786205472
Exacrs786205472
Varsomers786205472
Maprs786205472
PheGenIrs786205472
hapmaprs786205472
1000 genomesrs786205472
hgdprs786205472
ensemblrs786205472
gopubmedrs786205472
geneviewrs786205472
scholarrs786205472
googlers786205472
pharmgkbrs786205472
gwascentralrs786205472
openSNPrs786205472
23andMers786205472
23andMe allrs786205472
SNP Nexus

SNPshotrs786205472
SNPdbers786205472
MSV3drs786205472
GWAS Ctlgrs786205472
Max Magnitude0
ClinVar
Risk rs786205472(C;C)
Alt rs786205472(C;C)
Reference rs786205472(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFRP C1QTNF5
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.119216197C>G
CLNSRC
CLNACC RCV000171202.1,