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rs863223989

From SNPedia

Orientationminus
Make rs863223989(-;-)
Make rs863223989(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241500564
GeneFH
is asnp
is mentioned by
dbSNPrs863223989
ebirs863223989
HLIrs863223989
Exacrs863223989
Varsomers863223989
Maprs863223989
PheGenIrs863223989
hapmaprs863223989
1000 genomesrs863223989
hgdprs863223989
ensemblrs863223989
gopubmedrs863223989
geneviewrs863223989
scholarrs863223989
googlers863223989
pharmgkbrs863223989
gwascentralrs863223989
openSNPrs863223989
23andMers863223989
23andMe allrs863223989
SNP Nexus

SNPshotrs863223989
SNPdbers863223989
MSV3drs863223989
GWAS Ctlgrs863223989
Max Magnitude
ClinVar
Risk rs863223989(;)
Alt rs863223989(;)
Reference rs863223989(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241663864delC
CLNSRC
CLNACC RCV000196430.1,