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rs368924997

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368924997(A;A)
Make rs368924997(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position144360935
GeneSLC52A2
is asnp
is mentioned by
dbSNPrs368924997
ebirs368924997
HLIrs368924997
Exacrs368924997
Varsomers368924997
Maprs368924997
PheGenIrs368924997
hapmaprs368924997
1000 genomesrs368924997
hgdprs368924997
ensemblrs368924997
gopubmedrs368924997
geneviewrs368924997
scholarrs368924997
googlers368924997
pharmgkbrs368924997
gwascentralrs368924997
openSNPrs368924997
23andMers368924997
23andMe allrs368924997
SNP Nexus

SNPshotrs368924997
SNPdbers368924997
MSV3drs368924997
GWAS Ctlgrs368924997
Max Magnitude0
ClinVar
Risk rs368924997(A;A)
Alt rs368924997(A;A)
Reference rs368924997(G;G)
Significance Pathogenic
Disease Brown-Vialetto-Van Laere syndrome 2 not provided
Variation info
Gene SLC52A2
CLNDBN Brown-Vialetto-Van Laere syndrome 2 not provided
Reversed 0
HGVS NC_000008.10:g.145584595G>A
CLNSRC
CLNACC RCV000191988.1, RCV000237019.1,