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rs727503927

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727503927(A;A)
Make rs727503927(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position241504083
GeneFH
is asnp
is mentioned by
dbSNPrs727503927
ebirs727503927
HLIrs727503927
Exacrs727503927
Varsomers727503927
Maprs727503927
PheGenIrs727503927
hapmaprs727503927
1000 genomesrs727503927
hgdprs727503927
ensemblrs727503927
gopubmedrs727503927
geneviewrs727503927
scholarrs727503927
googlers727503927
pharmgkbrs727503927
gwascentralrs727503927
openSNPrs727503927
23andMers727503927
23andMe allrs727503927
SNP Nexus

SNPshotrs727503927
SNPdbers727503927
MSV3drs727503927
GWAS Ctlgrs727503927
Max Magnitude0
ClinVar
Risk rs727503927(A;A)
Alt rs727503927(A;A)
Reference rs727503927(T;T)
Significance Pathogenic
Disease not provided Hereditary leiomyomatosis and renal cell cancer
Variation info
Gene FH
CLNDBN not provided Hereditary leiomyomatosis and renal cell cancer
Reversed 1
HGVS NC_000001.10:g.241667383A>T
CLNSRC
CLNACC RCV000153235.3, RCV000190645.1,