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rs1060499641

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499641(-;-)
Make rs1060499641(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241504109
GeneFH
is asnp
is mentioned by
dbSNPrs1060499641
dbSNP (old)rs1060499641
ClinGenrs1060499641
ebirs1060499641
HLIrs1060499641
Exacrs1060499641
Gnomadrs1060499641
Varsomers1060499641
Maprs1060499641
PheGenIrs1060499641
Biobankrs1060499641
1000 genomesrs1060499641
hgdprs1060499641
ensemblrs1060499641
gopubmedrs1060499641
geneviewrs1060499641
scholarrs1060499641
googlers1060499641
pharmgkbrs1060499641
gwascentralrs1060499641
openSNPrs1060499641
23andMers1060499641
23andMe allrs1060499641
SNPshotrs1060499641
SNPdbers1060499641
MSV3drs1060499641
GWAS Ctlgrs1060499641
Max Magnitude0
ClinVar
Risk rs1060499641(-;-)
Alt rs1060499641(-;-)
Reference Rs1060499641(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.241667409delA
CLNSRC
CLNACC RCV000445598.1,