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rs369399450

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369399450(C;T)
Make rs369399450(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position158662673
GeneGFM1
is asnp
is mentioned by
dbSNPrs369399450
ebirs369399450
HLIrs369399450
Exacrs369399450
Varsomers369399450
Maprs369399450
PheGenIrs369399450
hapmaprs369399450
1000 genomesrs369399450
hgdprs369399450
ensemblrs369399450
gopubmedrs369399450
geneviewrs369399450
scholarrs369399450
googlers369399450
pharmgkbrs369399450
gwascentralrs369399450
openSNPrs369399450
23andMers369399450
23andMe allrs369399450
SNP Nexus

SNPshotrs369399450
SNPdbers369399450
MSV3drs369399450
GWAS Ctlgrs369399450
Max Magnitude0
ClinVar
Risk rs369399450(T;T)
Alt rs369399450(T;T)
Reference rs369399450(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GFM1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.158380462C>T
CLNSRC
CLNACC RCV000195753.1,