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rs879255540

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs879255540(-;-)
Make rs879255540(-;T)
Make rs879255540(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position19008000
GeneADGRG2, LOC101928415
is asnp
is mentioned by
dbSNPrs879255540
ebirs879255540
HLIrs879255540
Exacrs879255540
Varsomers879255540
Maprs879255540
PheGenIrs879255540
hapmaprs879255540
1000 genomesrs879255540
hgdprs879255540
ensemblrs879255540
gopubmedrs879255540
geneviewrs879255540
scholarrs879255540
googlers879255540
pharmgkbrs879255540
gwascentralrs879255540
openSNPrs879255540
23andMers879255540
23andMe allrs879255540
SNP Nexus

SNPshotrs879255540
SNPdbers879255540
MSV3drs879255540
GWAS Ctlgrs879255540
Max Magnitude0
ClinVar
Risk rs879255540(T;T)
Alt rs879255540(T;T)
Reference rs879255540(;)
Significance Pathogenic
Disease Congenital bilateral absence of the vas deferens
Variation info
Gene ADGRG2 LOC101928415
CLNDBN Congenital bilateral absence of the vas deferens
Reversed 1
HGVS NC_000023.10:g.19026119dupA
CLNSRC
CLNACC RCV000239604.1,