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rs201845396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201845396(C;T)
Make rs201845396(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position31545856
GeneDSG2, DSG2-AS1
is asnp
is mentioned by
dbSNPrs201845396
dbSNP (classic)rs201845396
ClinGenrs201845396
ebirs201845396
HLIrs201845396
Exacrs201845396
Gnomadrs201845396
Varsomers201845396
LitVarrs201845396
Maprs201845396
PheGenIrs201845396
Biobankrs201845396
1000 genomesrs201845396
hgdprs201845396
ensemblrs201845396
geneviewrs201845396
scholarrs201845396
googlers201845396
pharmgkbrs201845396
gwascentralrs201845396
openSNPrs201845396
23andMers201845396
SNPshotrs201845396
SNPdbers201845396
MSV3drs201845396
GWAS Ctlgrs201845396
Max Magnitude0
ClinVar
Risk rs201845396(G;G) rs201845396(T;T)
Alt rs201845396(G;G) rs201845396(T;T)
Reference Rs201845396(C;C)
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.29125819C>T
CLNSRC
CLNACC RCV000219803.1, RCV000489296.1,