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rs587782618

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782618(A;A)
Make rs587782618(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position241508784
GeneFH
is asnp
is mentioned by
dbSNPrs587782618
ebirs587782618
HLIrs587782618
Exacrs587782618
Varsomers587782618
Maprs587782618
PheGenIrs587782618
hapmaprs587782618
1000 genomesrs587782618
hgdprs587782618
ensemblrs587782618
gopubmedrs587782618
geneviewrs587782618
scholarrs587782618
googlers587782618
pharmgkbrs587782618
gwascentralrs587782618
openSNPrs587782618
23andMers587782618
23andMe allrs587782618
SNP Nexus

SNPshotrs587782618
SNPdbers587782618
MSV3drs587782618
GWAS Ctlgrs587782618
Max Magnitude0
ClinVar
Risk rs587782618(A;A)
Alt rs587782618(A;A)
Reference rs587782618(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene FH
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.241672084C>T
CLNSRC
CLNACC RCV000131997.2,