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rs75086406

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
(G;G) 0 common in clinvar
Make rs75086406(C;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position241513679
GeneFH
is asnp
is mentioned by
dbSNPrs75086406
ebirs75086406
HLIrs75086406
Exacrs75086406
Varsomers75086406
Maprs75086406
PheGenIrs75086406
hapmaprs75086406
1000 genomesrs75086406
hgdprs75086406
ensemblrs75086406
gopubmedrs75086406
geneviewrs75086406
scholarrs75086406
googlers75086406
pharmgkbrs75086406
gwascentralrs75086406
openSNPrs75086406
23andMers75086406
23andMe allrs75086406
SNP Nexus

SNPshotrs75086406
SNPdbers75086406
MSV3drs75086406
GWAS Ctlgrs75086406
GMAF0.0004591
Max Magnitude0
OMIM136850
Desc
Variant0009
Relatedalso
ClinVar
Risk rs75086406(A,C;A,C)
Alt rs75086406(A,C;A,C)
Reference rs75086406(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.241676979C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017625.29,