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rs748902766

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs748902766(A;G)
Make rs748902766(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position9972126
GeneNMNAT1
is asnp
is mentioned by
dbSNPrs748902766
ebirs748902766
HLIrs748902766
Exacrs748902766
Varsomers748902766
Maprs748902766
PheGenIrs748902766
hapmaprs748902766
1000 genomesrs748902766
hgdprs748902766
ensemblrs748902766
gopubmedrs748902766
geneviewrs748902766
scholarrs748902766
googlers748902766
pharmgkbrs748902766
gwascentralrs748902766
openSNPrs748902766
23andMers748902766
23andMe allrs748902766
SNP Nexus

SNPshotrs748902766
SNPdbers748902766
MSV3drs748902766
GWAS Ctlgrs748902766
Max Magnitude0
ClinVar
Risk rs748902766(G;G)
Alt rs748902766(G;G)
Reference rs748902766(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NMNAT1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.10032184A>G
CLNSRC
CLNACC RCV000171148.1,