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rs863223971

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223971(A;A)
Make rs863223971(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241504174
GeneFH
is asnp
is mentioned by
dbSNPrs863223971
ebirs863223971
HLIrs863223971
Exacrs863223971
Varsomers863223971
Maprs863223971
PheGenIrs863223971
hapmaprs863223971
1000 genomesrs863223971
hgdprs863223971
ensemblrs863223971
gopubmedrs863223971
geneviewrs863223971
scholarrs863223971
googlers863223971
pharmgkbrs863223971
gwascentralrs863223971
openSNPrs863223971
23andMers863223971
23andMe allrs863223971
SNP Nexus

SNPshotrs863223971
SNPdbers863223971
MSV3drs863223971
GWAS Ctlgrs863223971
Max Magnitude0
ClinVar
Risk rs863223971(A;A)
Alt rs863223971(A;A)
Reference rs863223971(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241667474C>T
CLNSRC
CLNACC RCV000196076.1,