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rs576404380

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs576404380(A;G)
Make rs576404380(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position31535365
GeneDSG2
is asnp
is mentioned by
dbSNPrs576404380
ebirs576404380
HLIrs576404380
Exacrs576404380
Varsomers576404380
Maprs576404380
PheGenIrs576404380
hapmaprs576404380
1000 genomesrs576404380
hgdprs576404380
ensemblrs576404380
gopubmedrs576404380
geneviewrs576404380
scholarrs576404380
googlers576404380
pharmgkbrs576404380
gwascentralrs576404380
openSNPrs576404380
23andMers576404380
23andMe allrs576404380
SNP Nexus

SNPshotrs576404380
SNPdbers576404380
MSV3drs576404380
GWAS Ctlgrs576404380
Max Magnitude0
ClinVar
Risk rs576404380(G;G)
Alt rs576404380(G;G)
Reference rs576404380(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSG2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29115328A>G
CLNSRC
CLNACC RCV000171268.1,