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rs747768373

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs747768373(A;A)
Make rs747768373(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position109792665
GeneFIG4
is asnp
is mentioned by
dbSNPrs747768373
ebirs747768373
HLIrs747768373
Exacrs747768373
Varsomers747768373
Maprs747768373
PheGenIrs747768373
hapmaprs747768373
1000 genomesrs747768373
hgdprs747768373
ensemblrs747768373
gopubmedrs747768373
geneviewrs747768373
scholarrs747768373
googlers747768373
pharmgkbrs747768373
gwascentralrs747768373
openSNPrs747768373
23andMers747768373
23andMe allrs747768373
SNP Nexus

SNPshotrs747768373
SNPdbers747768373
MSV3drs747768373
GWAS Ctlgrs747768373
Max Magnitude0
ClinVar
Risk rs747768373(A;A)
Alt rs747768373(A;A)
Reference rs747768373(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FIG4
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.110113868G>A
CLNSRC
CLNACC RCV000236022.1,