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rs371146201

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs371146201(A;A)
Make rs371146201(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position31542823
GeneDSG2, DSG2-AS1
is asnp
is mentioned by
dbSNPrs371146201
ebirs371146201
HLIrs371146201
Exacrs371146201
Varsomers371146201
Maprs371146201
PheGenIrs371146201
hapmaprs371146201
1000 genomesrs371146201
hgdprs371146201
ensemblrs371146201
gopubmedrs371146201
geneviewrs371146201
scholarrs371146201
googlers371146201
pharmgkbrs371146201
gwascentralrs371146201
openSNPrs371146201
23andMers371146201
23andMe allrs371146201
SNP Nexus

SNPshotrs371146201
SNPdbers371146201
MSV3drs371146201
GWAS Ctlgrs371146201
Max Magnitude0
ClinVar
Risk rs371146201(A;A)
Alt rs371146201(A;A)
Reference rs371146201(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene DSG2-AS1 DSG2
CLNDBN not specified not provided
Reversed 0
HGVS NC_000018.9:g.29122786G>A
CLNSRC
CLNACC RCV000150543.1, RCV000171269.1,