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rs1060499645

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499645(-;-)
Make rs1060499645(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241497892
GeneFH
is asnp
is mentioned by
dbSNPrs1060499645
dbSNP (old)rs1060499645
ClinGenrs1060499645
ebirs1060499645
HLIrs1060499645
Exacrs1060499645
Gnomadrs1060499645
Varsomers1060499645
Maprs1060499645
PheGenIrs1060499645
Biobankrs1060499645
1000 genomesrs1060499645
hgdprs1060499645
ensemblrs1060499645
gopubmedrs1060499645
geneviewrs1060499645
scholarrs1060499645
googlers1060499645
pharmgkbrs1060499645
gwascentralrs1060499645
openSNPrs1060499645
23andMers1060499645
23andMe allrs1060499645
SNPshotrs1060499645
SNPdbers1060499645
MSV3drs1060499645
GWAS Ctlgrs1060499645
Max Magnitude0
ClinVar
Risk rs1060499645(-;-)
Alt rs1060499645(-;-)
Reference Rs1060499645(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.241661192delC
CLNSRC
CLNACC RCV000445610.1,