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rs1060499644

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499644(-;-)
Make rs1060499644(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241502470
GeneFH
is asnp
is mentioned by
dbSNPrs1060499644
dbSNP (old)rs1060499644
ClinGenrs1060499644
ebirs1060499644
HLIrs1060499644
Exacrs1060499644
Gnomadrs1060499644
Varsomers1060499644
LitVarrs1060499644
Maprs1060499644
PheGenIrs1060499644
Biobankrs1060499644
1000 genomesrs1060499644
hgdprs1060499644
ensemblrs1060499644
gopubmedrs1060499644
geneviewrs1060499644
scholarrs1060499644
googlers1060499644
pharmgkbrs1060499644
gwascentralrs1060499644
openSNPrs1060499644
23andMers1060499644
23andMe allrs1060499644
SNPshotrs1060499644
SNPdbers1060499644
MSV3drs1060499644
GWAS Ctlgrs1060499644
Max Magnitude0
ClinVar
Risk rs1060499644(-;-)
Alt rs1060499644(-;-)
Reference Rs1060499644(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.241665770delA
CLNSRC
CLNACC RCV000445613.1,