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rs774456344

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs774456344(A;A)
Make rs774456344(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position158649156
GeneGFM1
is asnp
is mentioned by
dbSNPrs774456344
ebirs774456344
HLIrs774456344
Exacrs774456344
Varsomers774456344
Maprs774456344
PheGenIrs774456344
hapmaprs774456344
1000 genomesrs774456344
hgdprs774456344
ensemblrs774456344
gopubmedrs774456344
geneviewrs774456344
scholarrs774456344
googlers774456344
pharmgkbrs774456344
gwascentralrs774456344
openSNPrs774456344
23andMers774456344
23andMe allrs774456344
SNP Nexus

SNPshotrs774456344
SNPdbers774456344
MSV3drs774456344
GWAS Ctlgrs774456344
Max Magnitude0
ClinVar
Risk rs774456344(A;A)
Alt rs774456344(A;A)
Reference rs774456344(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GFM1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.158366945G>A
CLNSRC
CLNACC RCV000199744.2,