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rs786200875

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786200875(-;-)
Make rs786200875(-;T)
Make rs786200875(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31409556
GeneDSG1-AS1, DSG4
is asnp
is mentioned by
dbSNPrs786200875
ebirs786200875
HLIrs786200875
Exacrs786200875
Varsomers786200875
Maprs786200875
PheGenIrs786200875
hapmaprs786200875
1000 genomesrs786200875
hgdprs786200875
ensemblrs786200875
gopubmedrs786200875
geneviewrs786200875
scholarrs786200875
googlers786200875
pharmgkbrs786200875
gwascentralrs786200875
openSNPrs786200875
23andMers786200875
23andMe allrs786200875
SNP Nexus

SNPshotrs786200875
SNPdbers786200875
MSV3drs786200875
GWAS Ctlgrs786200875
Max Magnitude0
ClinVar
Risk rs786200875(T;T)
Alt rs786200875(T;T)
Reference rs786200875(;)
Significance Pathogenic
Disease Hypotrichosis 6
Variation info
Gene DSG1-AS1 DSG4
CLNDBN Hypotrichosis 6
Reversed 0
HGVS NC_000018.9:g.28989519dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000002841.3,