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rs794728106

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728106(A;A)
Make rs794728106(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7555821
GeneDSP
is asnp
is mentioned by
dbSNPrs794728106
ebirs794728106
HLIrs794728106
Exacrs794728106
Varsomers794728106
Maprs794728106
PheGenIrs794728106
hapmaprs794728106
1000 genomesrs794728106
hgdprs794728106
ensemblrs794728106
gopubmedrs794728106
geneviewrs794728106
scholarrs794728106
googlers794728106
pharmgkbrs794728106
gwascentralrs794728106
openSNPrs794728106
23andMers794728106
23andMe allrs794728106
SNP Nexus

SNPshotrs794728106
SNPdbers794728106
MSV3drs794728106
GWAS Ctlgrs794728106
Max Magnitude0
ClinVar
Risk rs794728106(A;A)
Alt rs794728106(A;A)
Reference rs794728106(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7556054G>A
CLNSRC
CLNACC RCV000181270.1,