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rs1060499642

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499642(G;T)
Make rs1060499642(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241504087
GeneFH
is asnp
is mentioned by
dbSNPrs1060499642
dbSNP (classic)rs1060499642
ClinGenrs1060499642
ebirs1060499642
HLIrs1060499642
Exacrs1060499642
Gnomadrs1060499642
Varsomers1060499642
LitVarrs1060499642
Maprs1060499642
PheGenIrs1060499642
Biobankrs1060499642
1000 genomesrs1060499642
hgdprs1060499642
ensemblrs1060499642
geneviewrs1060499642
scholarrs1060499642
googlers1060499642
pharmgkbrs1060499642
gwascentralrs1060499642
openSNPrs1060499642
23andMers1060499642
23andMe allrs1060499642
SNPshotrs1060499642
SNPdbers1060499642
MSV3drs1060499642
GWAS Ctlgrs1060499642
Max Magnitude0
ClinVar
Risk rs1060499642(T;T)
Alt rs1060499642(T;T)
Reference Rs1060499642(G;G)
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.241667387C>A
CLNSRC
CLNACC RCV000445617.1,