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rs863224035

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224035(C;T)
Make rs863224035(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position158666368
GeneGFM1, LXN
is asnp
is mentioned by
dbSNPrs863224035
ebirs863224035
HLIrs863224035
Exacrs863224035
Varsomers863224035
Maprs863224035
PheGenIrs863224035
hapmaprs863224035
1000 genomesrs863224035
hgdprs863224035
ensemblrs863224035
gopubmedrs863224035
geneviewrs863224035
scholarrs863224035
googlers863224035
pharmgkbrs863224035
gwascentralrs863224035
openSNPrs863224035
23andMers863224035
23andMe allrs863224035
SNP Nexus

SNPshotrs863224035
SNPdbers863224035
MSV3drs863224035
GWAS Ctlgrs863224035
Max Magnitude0
ClinVar
Risk rs863224035(T;T)
Alt rs863224035(T;T)
Reference rs863224035(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GFM1 LXN
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.158384157C>T
CLNSRC
CLNACC RCV000200666.1,