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rs863223991

From SNPedia

Orientationminus
Make rs863223991(-;-)
Make rs863223991(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241500469
GeneFH
is asnp
is mentioned by
dbSNPrs863223991
ClinGenrs863223991
ebirs863223991
HLIrs863223991
Exacrs863223991
Varsomers863223991
Maprs863223991
PheGenIrs863223991
hapmaprs863223991
1000 genomesrs863223991
hgdprs863223991
ensemblrs863223991
gopubmedrs863223991
geneviewrs863223991
scholarrs863223991
googlers863223991
pharmgkbrs863223991
gwascentralrs863223991
openSNPrs863223991
23andMers863223991
23andMe allrs863223991
SNP Nexus

SNPshotrs863223991
SNPdbers863223991
MSV3drs863223991
GWAS Ctlgrs863223991
Max Magnitude
ClinVar
Risk
Alt
Reference Rs863223991(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241663769_241663770delAG
CLNSRC
CLNACC RCV000197139.1,