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rs863224017

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TTGAAGC;TTGAAGC) 0 common in clinvar
Make rs863224017(-;-)
Make rs863224017(-;TTGAAGC)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241513680
GeneFH
is asnp
is mentioned by
dbSNPrs863224017
dbSNP (old)rs863224017
ClinGenrs863224017
ebirs863224017
HLIrs863224017
Exacrs863224017
Gnomadrs863224017
Varsomers863224017
Maprs863224017
PheGenIrs863224017
Biobankrs863224017
1000 genomesrs863224017
hgdprs863224017
ensemblrs863224017
gopubmedrs863224017
geneviewrs863224017
scholarrs863224017
googlers863224017
pharmgkbrs863224017
gwascentralrs863224017
openSNPrs863224017
23andMers863224017
23andMe allrs863224017
SNP Nexus

SNPshotrs863224017
SNPdbers863224017
MSV3drs863224017
GWAS Ctlgrs863224017
Max Magnitude0
ClinVar
Risk rs863224017(-;-)
Alt rs863224017(-;-)
Reference Rs863224017(TTGAAGC;TTGAAGC)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241676980_241676986delGCTTCAA
CLNSRC
CLNACC RCV000199584.1,