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rs863223990

From SNPedia

Orientationminus
Make rs863223990(-;-)
Make rs863223990(-;ATGA)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241500475
GeneFH
is asnp
is mentioned by
dbSNPrs863223990
ebirs863223990
HLIrs863223990
Exacrs863223990
Varsomers863223990
Maprs863223990
PheGenIrs863223990
hapmaprs863223990
1000 genomesrs863223990
hgdprs863223990
ensemblrs863223990
gopubmedrs863223990
geneviewrs863223990
scholarrs863223990
googlers863223990
pharmgkbrs863223990
gwascentralrs863223990
openSNPrs863223990
23andMers863223990
23andMe allrs863223990
SNP Nexus

SNPshotrs863223990
SNPdbers863223990
MSV3drs863223990
GWAS Ctlgrs863223990
Max Magnitude
ClinVar
Risk rs863223990(;)
Alt rs863223990(;)
Reference rs863223990(ATGA;ATGA)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241663775_241663778delTCAT
CLNSRC
CLNACC RCV000200843.1,