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rs539821357

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs539821357(A;A)
Make rs539821357(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position31546425
GeneDSG2, DSG2-AS1
is asnp
is mentioned by
dbSNPrs539821357
dbSNP (classic)rs539821357
ClinGenrs539821357
ebirs539821357
HLIrs539821357
Exacrs539821357
Gnomadrs539821357
Varsomers539821357
LitVarrs539821357
Maprs539821357
PheGenIrs539821357
Biobankrs539821357
1000 genomesrs539821357
hgdprs539821357
ensemblrs539821357
geneviewrs539821357
scholarrs539821357
googlers539821357
pharmgkbrs539821357
gwascentralrs539821357
openSNPrs539821357
23andMers539821357
SNPshotrs539821357
SNPdbers539821357
MSV3drs539821357
GWAS Ctlgrs539821357
Max Magnitude0
ClinVar
Risk rs539821357(A;A) rs539821357(T;T)
Alt rs539821357(A;A) rs539821357(T;T)
Reference Rs539821357(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSG2-AS1 DSG2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29126388C>A
CLNSRC
CLNACC RCV000431080.1,