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rs1060499638

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499638(C;C)
Make rs1060499638(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241506087
GeneFH
is asnp
is mentioned by
dbSNPrs1060499638
dbSNP (old)rs1060499638
ClinGenrs1060499638
ebirs1060499638
HLIrs1060499638
Exacrs1060499638
Gnomadrs1060499638
Varsomers1060499638
Maprs1060499638
PheGenIrs1060499638
Biobankrs1060499638
1000 genomesrs1060499638
hgdprs1060499638
ensemblrs1060499638
gopubmedrs1060499638
geneviewrs1060499638
scholarrs1060499638
googlers1060499638
pharmgkbrs1060499638
gwascentralrs1060499638
openSNPrs1060499638
23andMers1060499638
23andMe allrs1060499638
SNPshotrs1060499638
SNPdbers1060499638
MSV3drs1060499638
GWAS Ctlgrs1060499638
Max Magnitude0
ClinVar
Risk rs1060499638(C;C)
Alt rs1060499638(C;C)
Reference Rs1060499638(G;G)
Significance Probable-Pathogenic
Disease Hereditary leiomyomatosis and renal cell cancer
Variation info
Gene FH
CLNDBN Hereditary leiomyomatosis and renal cell cancer
Reversed 1
HGVS NC_000001.10:g.241669387C>G
CLNSRC
CLNACC RCV000445594.1,