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rs67870244

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs67870244(C;G)
Make rs67870244(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411900
GeneOTC
is asnp
is mentioned by
dbSNPrs67870244
ebirs67870244
HLIrs67870244
Exacrs67870244
Varsomers67870244
Maprs67870244
PheGenIrs67870244
hapmaprs67870244
1000 genomesrs67870244
hgdprs67870244
ensemblrs67870244
gopubmedrs67870244
geneviewrs67870244
scholarrs67870244
googlers67870244
pharmgkbrs67870244
gwascentralrs67870244
openSNPrs67870244
23andMers67870244
23andMe allrs67870244
SNP Nexus

SNPshotrs67870244
SNPdbers67870244
MSV3drs67870244
GWAS Ctlgrs67870244
Max Magnitude0
ClinVar
Risk rs67870244(G;G)
Alt rs67870244(G;G)
Reference rs67870244(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271153C>G
CLNSRC ClinVar
CLNACC RCV000083602.1,