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rs7772593

From SNPedia

Orientationplus
Stabilizedplus
Make rs7772593(C;C)
Make rs7772593(C;T)
Make rs7772593(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position105897182
is asnp
is mentioned by
dbSNPrs7772593
dbSNP (old)rs7772593
ClinGenrs7772593
ebirs7772593
HLIrs7772593
Exacrs7772593
Gnomadrs7772593
Varsomers7772593
Maprs7772593
PheGenIrs7772593
Biobankrs7772593
1000 genomesrs7772593
hgdprs7772593
ensemblrs7772593
gopubmedrs7772593
geneviewrs7772593
scholarrs7772593
googlers7772593
pharmgkbrs7772593
gwascentralrs7772593
openSNPrs7772593
23andMers7772593
23andMe allrs7772593
SNP Nexus

SNPshotrs7772593
SNPdbers7772593
MSV3drs7772593
GWAS Ctlgrs7772593
GMAF0.1134
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19922138] Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis