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rs1060499636

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499636(G;G)
Make rs1060499636(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241508610
GeneFH
is asnp
is mentioned by
dbSNPrs1060499636
dbSNP (old)rs1060499636
ClinGenrs1060499636
ebirs1060499636
HLIrs1060499636
Exacrs1060499636
Gnomadrs1060499636
Varsomers1060499636
Maprs1060499636
PheGenIrs1060499636
Biobankrs1060499636
1000 genomesrs1060499636
hgdprs1060499636
ensemblrs1060499636
gopubmedrs1060499636
geneviewrs1060499636
scholarrs1060499636
googlers1060499636
pharmgkbrs1060499636
gwascentralrs1060499636
openSNPrs1060499636
23andMers1060499636
23andMe allrs1060499636
SNPshotrs1060499636
SNPdbers1060499636
MSV3drs1060499636
GWAS Ctlgrs1060499636
Max Magnitude0
ClinVar
Risk rs1060499636(G;G)
Alt rs1060499636(G;G)
Reference Rs1060499636(T;T)
Significance Probable-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.241671910A>C
CLNSRC
CLNACC RCV000445612.1,