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rs793888525

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs793888525(A;A)
Make rs793888525(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position142408187
GeneADGRG6
is asnp
is mentioned by
dbSNPrs793888525
ebirs793888525
HLIrs793888525
Exacrs793888525
Varsomers793888525
Maprs793888525
PheGenIrs793888525
hapmaprs793888525
1000 genomesrs793888525
hgdprs793888525
ensemblrs793888525
gopubmedrs793888525
geneviewrs793888525
scholarrs793888525
googlers793888525
pharmgkbrs793888525
gwascentralrs793888525
openSNPrs793888525
23andMers793888525
23andMe allrs793888525
SNP Nexus

SNPshotrs793888525
SNPdbers793888525
MSV3drs793888525
GWAS Ctlgrs793888525
Max Magnitude0
ClinVar
Risk rs793888525(A;A)
Alt rs793888525(A;A)
Reference rs793888525(T;T)
Significance Pathogenic
Disease Arthrogryposis multiplex congenita Lethal congenital contracture syndrome 9
Variation info
Gene GPR126 ADGRG6
CLNDBN Arthrogryposis multiplex congenita Lethal congenital contracture syndrome 9
Reversed 0
HGVS NC_000006.11:g.142729324T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000172979.1, RCV000186600.2,