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rs369610897

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369610897(C;G)
Make rs369610897(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position84449740
GeneSUCLG1
is asnp
is mentioned by
dbSNPrs369610897
ebirs369610897
HLIrs369610897
Exacrs369610897
Varsomers369610897
Maprs369610897
PheGenIrs369610897
hapmaprs369610897
1000 genomesrs369610897
hgdprs369610897
ensemblrs369610897
gopubmedrs369610897
geneviewrs369610897
scholarrs369610897
googlers369610897
pharmgkbrs369610897
gwascentralrs369610897
openSNPrs369610897
23andMers369610897
23andMe allrs369610897
SNP Nexus

SNPshotrs369610897
SNPdbers369610897
MSV3drs369610897
GWAS Ctlgrs369610897
Max Magnitude0
ClinVar
Risk rs369610897(G;G)
Alt rs369610897(G;G)
Reference rs369610897(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene SUCLG1
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.84676864C>G
CLNSRC
CLNACC RCV000186193.2,