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rs771599779

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771599779(A;A)
Make rs771599779(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position47996909
GeneSUCLA2
is asnp
is mentioned by
dbSNPrs771599779
ebirs771599779
HLIrs771599779
Exacrs771599779
Varsomers771599779
Maprs771599779
PheGenIrs771599779
hapmaprs771599779
1000 genomesrs771599779
hgdprs771599779
ensemblrs771599779
gopubmedrs771599779
geneviewrs771599779
scholarrs771599779
googlers771599779
pharmgkbrs771599779
gwascentralrs771599779
openSNPrs771599779
23andMers771599779
23andMe allrs771599779
SNP Nexus

SNPshotrs771599779
SNPdbers771599779
MSV3drs771599779
GWAS Ctlgrs771599779
Max Magnitude0
ClinVar
Risk rs771599779(A;A)
Alt rs771599779(A;A)
Reference rs771599779(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SUCLA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.48571044C>A
CLNSRC
CLNACC RCV000186189.1,