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rs879255538

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs879255538(-;-)
Make rs879255538(-;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position18994920
GeneADGRG2, LOC101928415
is asnp
is mentioned by
dbSNPrs879255538
dbSNP (old)rs879255538
ClinGenrs879255538
ebirs879255538
HLIrs879255538
Exacrs879255538
Gnomadrs879255538
Varsomers879255538
Maprs879255538
PheGenIrs879255538
Biobankrs879255538
1000 genomesrs879255538
hgdprs879255538
ensemblrs879255538
gopubmedrs879255538
geneviewrs879255538
scholarrs879255538
googlers879255538
pharmgkbrs879255538
gwascentralrs879255538
openSNPrs879255538
23andMers879255538
23andMe allrs879255538
SNP Nexus

SNPshotrs879255538
SNPdbers879255538
MSV3drs879255538
GWAS Ctlgrs879255538
Max Magnitude0
ClinVar
Risk rs879255538(-;-)
Alt rs879255538(-;-)
Reference Rs879255538(T;T)
Significance Pathogenic
Disease Congenital bilateral absence of the vas deferens Vas deferens
Variation info
Gene ADGRG2 LOC101928415
CLNDBN Congenital bilateral absence of the vas deferens Vas deferens, congenital bilateral aplasia of, X-linked
Reversed 1
HGVS NC_000023.10:g.19013038delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000239608.1, RCV000252079.1,