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rs1060499637

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499637(-;-)
Make rs1060499637(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241506099
GeneFH
is asnp
is mentioned by
dbSNPrs1060499637
dbSNP (old)rs1060499637
ClinGenrs1060499637
ebirs1060499637
HLIrs1060499637
Exacrs1060499637
Gnomadrs1060499637
Varsomers1060499637
LitVarrs1060499637
Maprs1060499637
PheGenIrs1060499637
Biobankrs1060499637
1000 genomesrs1060499637
hgdprs1060499637
ensemblrs1060499637
gopubmedrs1060499637
geneviewrs1060499637
scholarrs1060499637
googlers1060499637
pharmgkbrs1060499637
gwascentralrs1060499637
openSNPrs1060499637
23andMers1060499637
23andMe allrs1060499637
SNPshotrs1060499637
SNPdbers1060499637
MSV3drs1060499637
GWAS Ctlgrs1060499637
Max Magnitude0
ClinVar
Risk rs1060499637(-;-)
Alt rs1060499637(-;-)
Reference Rs1060499637(T;T)
Significance 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.241669399delA
CLNSRC
CLNACC RCV000445636.1,