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rs863224032

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224032(C;T)
Make rs863224032(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position158652106
GeneGFM1
is asnp
is mentioned by
dbSNPrs863224032
ebirs863224032
HLIrs863224032
Exacrs863224032
Varsomers863224032
Maprs863224032
PheGenIrs863224032
hapmaprs863224032
1000 genomesrs863224032
hgdprs863224032
ensemblrs863224032
gopubmedrs863224032
geneviewrs863224032
scholarrs863224032
googlers863224032
pharmgkbrs863224032
gwascentralrs863224032
openSNPrs863224032
23andMers863224032
23andMe allrs863224032
SNP Nexus

SNPshotrs863224032
SNPdbers863224032
MSV3drs863224032
GWAS Ctlgrs863224032
Max Magnitude0
ClinVar
Risk rs863224032(T;T)
Alt rs863224032(T;T)
Reference rs863224032(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GFM1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.158369895C>T
CLNSRC
CLNACC RCV000198570.1,