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rs773748583

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs773748583(A;C)
Make rs773748583(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position84443300
GeneSUCLG1
is asnp
is mentioned by
dbSNPrs773748583
ebirs773748583
HLIrs773748583
Exacrs773748583
Varsomers773748583
Maprs773748583
PheGenIrs773748583
hapmaprs773748583
1000 genomesrs773748583
hgdprs773748583
ensemblrs773748583
gopubmedrs773748583
geneviewrs773748583
scholarrs773748583
googlers773748583
pharmgkbrs773748583
gwascentralrs773748583
openSNPrs773748583
23andMers773748583
23andMe allrs773748583
SNP Nexus

SNPshotrs773748583
SNPdbers773748583
MSV3drs773748583
GWAS Ctlgrs773748583
Max Magnitude0
ClinVar
Risk rs773748583(C;C)
Alt rs773748583(C;C)
Reference rs773748583(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SUCLG1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.84670424A>C
CLNSRC
CLNACC RCV000186204.1,