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rs1060499643

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499643(A;G)
Make rs1060499643(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241502561
GeneFH
is asnp
is mentioned by
dbSNPrs1060499643
dbSNP (old)rs1060499643
ClinGenrs1060499643
ebirs1060499643
HLIrs1060499643
Exacrs1060499643
Gnomadrs1060499643
Varsomers1060499643
Maprs1060499643
PheGenIrs1060499643
Biobankrs1060499643
1000 genomesrs1060499643
hgdprs1060499643
ensemblrs1060499643
gopubmedrs1060499643
geneviewrs1060499643
scholarrs1060499643
googlers1060499643
pharmgkbrs1060499643
gwascentralrs1060499643
openSNPrs1060499643
23andMers1060499643
23andMe allrs1060499643
SNPshotrs1060499643
SNPdbers1060499643
MSV3drs1060499643
GWAS Ctlgrs1060499643
Max Magnitude0
ClinVar
Risk rs1060499643(G;G)
Alt rs1060499643(G;G)
Reference Rs1060499643(A;A)
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.241665861T>C
CLNSRC
CLNACC RCV000445626.1,