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rs370898100

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370898100(A;A)
Make rs370898100(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position47988596
GeneSUCLA2
is asnp
is mentioned by
dbSNPrs370898100
ebirs370898100
HLIrs370898100
Exacrs370898100
Varsomers370898100
Maprs370898100
PheGenIrs370898100
hapmaprs370898100
1000 genomesrs370898100
hgdprs370898100
ensemblrs370898100
gopubmedrs370898100
geneviewrs370898100
scholarrs370898100
googlers370898100
pharmgkbrs370898100
gwascentralrs370898100
openSNPrs370898100
23andMers370898100
23andMe allrs370898100
SNP Nexus

SNPshotrs370898100
SNPdbers370898100
MSV3drs370898100
GWAS Ctlgrs370898100
Max Magnitude0
ClinVar
Risk rs370898100(A,T;A,T)
Alt rs370898100(A,T;A,T)
Reference rs370898100(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SUCLA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.48562731C>T
CLNSRC
CLNACC RCV000186180.1,