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rs201751992

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs201751992(C;C)
Make rs201751992(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position78571419
GeneNARS2
is asnp
is mentioned by
dbSNPrs201751992
dbSNP (classic)rs201751992
ClinGenrs201751992
ebirs201751992
HLIrs201751992
Exacrs201751992
Gnomadrs201751992
Varsomers201751992
LitVarrs201751992
Maprs201751992
PheGenIrs201751992
Biobankrs201751992
1000 genomesrs201751992
hgdprs201751992
ensemblrs201751992
geneviewrs201751992
scholarrs201751992
googlers201751992
pharmgkbrs201751992
gwascentralrs201751992
openSNPrs201751992
23andMers201751992
23andMe allrs201751992
SNPshotrs201751992
SNPdbers201751992
MSV3drs201751992
GWAS Ctlgrs201751992
Max Magnitude0
ClinVar
Risk rs201751992(C;C) rs201751992(G;G)
Alt rs201751992(C;C) rs201751992(G;G)
Reference Rs201751992(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NARS2
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.78282464T>C
CLNSRC
CLNACC RCV000481204.1,