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rs544389920

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs544389920(C;T)
Make rs544389920(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position158658952
GeneGFM1
is asnp
is mentioned by
dbSNPrs544389920
ebirs544389920
HLIrs544389920
Exacrs544389920
Varsomers544389920
Maprs544389920
PheGenIrs544389920
hapmaprs544389920
1000 genomesrs544389920
hgdprs544389920
ensemblrs544389920
gopubmedrs544389920
geneviewrs544389920
scholarrs544389920
googlers544389920
pharmgkbrs544389920
gwascentralrs544389920
openSNPrs544389920
23andMers544389920
23andMe allrs544389920
SNP Nexus

SNPshotrs544389920
SNPdbers544389920
MSV3drs544389920
GWAS Ctlgrs544389920
Max Magnitude0
ClinVar
Risk rs544389920(T;T)
Alt rs544389920(T;T)
Reference rs544389920(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GFM1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.158376741C>T
CLNSRC
CLNACC RCV000197604.1,