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rs749730642

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs749730642(C;C)
Make rs749730642(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7581151
GeneDSP
is asnp
is mentioned by
dbSNPrs749730642
ebirs749730642
HLIrs749730642
Exacrs749730642
Varsomers749730642
Maprs749730642
PheGenIrs749730642
hapmaprs749730642
1000 genomesrs749730642
hgdprs749730642
ensemblrs749730642
gopubmedrs749730642
geneviewrs749730642
scholarrs749730642
googlers749730642
pharmgkbrs749730642
gwascentralrs749730642
openSNPrs749730642
23andMers749730642
23andMe allrs749730642
SNP Nexus

SNPshotrs749730642
SNPdbers749730642
MSV3drs749730642
GWAS Ctlgrs749730642
Max Magnitude0
ClinVar
Risk rs749730642(C;C)
Alt rs749730642(C;C)
Reference rs749730642(T;T)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene DSP
CLNDBN not provided not specified
Reversed 0
HGVS NC_000006.11:g.7581384T>C
CLNSRC
CLNACC RCV000181322.1, RCV000219274.1,