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rs863223988

From SNPedia

Orientationminus
Make rs863223988(-;-)
Make rs863223988(-;TGAC)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241502537
GeneFH
is asnp
is mentioned by
dbSNPrs863223988
ebirs863223988
HLIrs863223988
Exacrs863223988
Varsomers863223988
Maprs863223988
PheGenIrs863223988
hapmaprs863223988
1000 genomesrs863223988
hgdprs863223988
ensemblrs863223988
gopubmedrs863223988
geneviewrs863223988
scholarrs863223988
googlers863223988
pharmgkbrs863223988
gwascentralrs863223988
openSNPrs863223988
23andMers863223988
23andMe allrs863223988
SNP Nexus

SNPshotrs863223988
SNPdbers863223988
MSV3drs863223988
GWAS Ctlgrs863223988
Max Magnitude
ClinVar
Risk rs863223988(;)
Alt rs863223988(;)
Reference rs863223988(TGAC;TGAC)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241665837_241665840delGTCA
CLNSRC
CLNACC RCV000199986.1,