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rs777573018

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs777573018(C;T)
Make rs777573018(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7583740
GeneDSP
is asnp
is mentioned by
dbSNPrs777573018
ebirs777573018
HLIrs777573018
Exacrs777573018
Varsomers777573018
Maprs777573018
PheGenIrs777573018
hapmaprs777573018
1000 genomesrs777573018
hgdprs777573018
ensemblrs777573018
gopubmedrs777573018
geneviewrs777573018
scholarrs777573018
googlers777573018
pharmgkbrs777573018
gwascentralrs777573018
openSNPrs777573018
23andMers777573018
23andMe allrs777573018
SNP Nexus

SNPshotrs777573018
SNPdbers777573018
MSV3drs777573018
GWAS Ctlgrs777573018
Max Magnitude0
ClinVar
Risk rs777573018(T;T)
Alt rs777573018(T;T)
Reference rs777573018(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7583973C>T
CLNSRC
CLNACC RCV000181341.1,