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rs768858918

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768858918(A;A)
Make rs768858918(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7577886
GeneDSP
is asnp
is mentioned by
dbSNPrs768858918
ebirs768858918
HLIrs768858918
Exacrs768858918
Varsomers768858918
Maprs768858918
PheGenIrs768858918
hapmaprs768858918
1000 genomesrs768858918
hgdprs768858918
ensemblrs768858918
gopubmedrs768858918
geneviewrs768858918
scholarrs768858918
googlers768858918
pharmgkbrs768858918
gwascentralrs768858918
openSNPrs768858918
23andMers768858918
23andMe allrs768858918
SNP Nexus

SNPshotrs768858918
SNPdbers768858918
MSV3drs768858918
GWAS Ctlgrs768858918
Max Magnitude0
ClinVar
Risk rs768858918(A;A)
Alt rs768858918(A;A)
Reference rs768858918(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7578119G>A
CLNSRC
CLNACC RCV000181311.2,