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rs727504738

From SNPedia

Orientationplus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs727504738(AGCTCGAGTCCCTCG;AGCTCGAGTCCCTCG)
Make rs727504738(AGCTCGAGTCCCTCG;CC)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7559294
GeneDSP
is asnp
is mentioned by
dbSNPrs727504738
ebirs727504738
HLIrs727504738
Exacrs727504738
Varsomers727504738
Maprs727504738
PheGenIrs727504738
hapmaprs727504738
1000 genomesrs727504738
hgdprs727504738
ensemblrs727504738
gopubmedrs727504738
geneviewrs727504738
scholarrs727504738
googlers727504738
pharmgkbrs727504738
gwascentralrs727504738
openSNPrs727504738
23andMers727504738
23andMe allrs727504738
SNP Nexus

SNPshotrs727504738
SNPdbers727504738
MSV3drs727504738
GWAS Ctlgrs727504738
Max Magnitude0
ClinVar
Risk rs727504738(AGCTCGAGTCCCTCG;AGCTCGAGTCCCTCG)
Alt rs727504738(AGCTCGAGTCCCTCG;AGCTCGAGTCCCTCG)
Reference rs727504738(CC;CC)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene DSP
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7559527_7559528delinsAGCTCGAGTCCCTCG
CLNSRC
CLNACC RCV000156036.1,