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rs786205471

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205471(A;A)
Make rs786205471(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position119344900
GeneC1QTNF5, MFRP
is asnp
is mentioned by
dbSNPrs786205471
ebirs786205471
HLIrs786205471
Exacrs786205471
Varsomers786205471
Maprs786205471
PheGenIrs786205471
hapmaprs786205471
1000 genomesrs786205471
hgdprs786205471
ensemblrs786205471
gopubmedrs786205471
geneviewrs786205471
scholarrs786205471
googlers786205471
pharmgkbrs786205471
gwascentralrs786205471
openSNPrs786205471
23andMers786205471
23andMe allrs786205471
SNP Nexus

SNPshotrs786205471
SNPdbers786205471
MSV3drs786205471
GWAS Ctlgrs786205471
Max Magnitude0
ClinVar
Risk rs786205471(A;A)
Alt rs786205471(A;A)
Reference rs786205471(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFRP C1QTNF5
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.119215610C>T
CLNSRC
CLNACC RCV000171201.1,