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rs397516912

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516912(A;C)
Make rs397516912(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7567421
GeneDSP
is asnp
is mentioned by
dbSNPrs397516912
ebirs397516912
HLIrs397516912
Exacrs397516912
Varsomers397516912
Maprs397516912
PheGenIrs397516912
hapmaprs397516912
1000 genomesrs397516912
hgdprs397516912
ensemblrs397516912
gopubmedrs397516912
geneviewrs397516912
scholarrs397516912
googlers397516912
pharmgkbrs397516912
gwascentralrs397516912
openSNPrs397516912
23andMers397516912
23andMe allrs397516912
SNP Nexus

SNPshotrs397516912
SNPdbers397516912
MSV3drs397516912
GWAS Ctlgrs397516912
Max Magnitude0
ClinVar
Risk rs397516912(C;C)
Alt rs397516912(C;C)
Reference rs397516912(A;A)
Significance Pathogenic
Disease not specified
Variation info
Gene DSP
CLNDBN not specified
Reversed 0
HGVS NC_000006.11:g.7567654A>C
CLNSRC
CLNACC RCV000037984.2,