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rs1060499634

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499634(-;-)
Make rs1060499634(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241511998
GeneFH
is asnp
is mentioned by
dbSNPrs1060499634
dbSNP (old)rs1060499634
ClinGenrs1060499634
ebirs1060499634
HLIrs1060499634
Exacrs1060499634
Gnomadrs1060499634
Varsomers1060499634
Maprs1060499634
PheGenIrs1060499634
Biobankrs1060499634
1000 genomesrs1060499634
hgdprs1060499634
ensemblrs1060499634
gopubmedrs1060499634
geneviewrs1060499634
scholarrs1060499634
googlers1060499634
pharmgkbrs1060499634
gwascentralrs1060499634
openSNPrs1060499634
23andMers1060499634
23andMe allrs1060499634
SNPshotrs1060499634
SNPdbers1060499634
MSV3drs1060499634
GWAS Ctlgrs1060499634
Max Magnitude0
ClinVar
Risk rs1060499634(-;-)
Alt rs1060499634(-;-)
Reference Rs1060499634(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.241675298delA
CLNSRC
CLNACC RCV000445619.1,