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rs727503928

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727503928(-;-)
Make rs727503928(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position241508604
GeneFH
is asnp
is mentioned by
dbSNPrs727503928
ebirs727503928
HLIrs727503928
Exacrs727503928
Varsomers727503928
Maprs727503928
PheGenIrs727503928
hapmaprs727503928
1000 genomesrs727503928
hgdprs727503928
ensemblrs727503928
gopubmedrs727503928
geneviewrs727503928
scholarrs727503928
googlers727503928
pharmgkbrs727503928
gwascentralrs727503928
openSNPrs727503928
23andMers727503928
23andMe allrs727503928
SNP Nexus

SNPshotrs727503928
SNPdbers727503928
MSV3drs727503928
GWAS Ctlgrs727503928
Max Magnitude0
ClinVar
Risk rs727503928(;)
Alt rs727503928(;)
Reference rs727503928(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241671904delT
CLNSRC
CLNACC RCV000153236.3,