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rs879253743

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879253743(C;G)
Make rs879253743(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position100975538
GeneLOC101927142, NPAS2
is asnp
is mentioned by
dbSNPrs879253743
ebirs879253743
HLIrs879253743
Exacrs879253743
Varsomers879253743
Maprs879253743
PheGenIrs879253743
hapmaprs879253743
1000 genomesrs879253743
hgdprs879253743
ensemblrs879253743
gopubmedrs879253743
geneviewrs879253743
scholarrs879253743
googlers879253743
pharmgkbrs879253743
gwascentralrs879253743
openSNPrs879253743
23andMers879253743
23andMe allrs879253743
SNP Nexus

SNPshotrs879253743
SNPdbers879253743
MSV3drs879253743
GWAS Ctlgrs879253743
Max Magnitude0
ClinVar
Risk rs879253743(G;G)
Alt rs879253743(G;G)
Reference rs879253743(C;C)
Significance Probable-Pathogenic
Disease Non-obstructive azoospermia
Variation info
Gene LOC101927142 NPAS2
CLNDBN Non-obstructive azoospermia
Reversed 0
HGVS NC_000002.11:g.101592000C>G
CLNSRC
CLNACC RCV000234891.1,