Have questions? Visit https://www.reddit.com/r/SNPedia

rs148579886

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148579886(A;A)
Make rs148579886(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position39909922
GeneMOCS1
is asnp
is mentioned by
dbSNPrs148579886
ebirs148579886
HLIrs148579886
Exacrs148579886
Varsomers148579886
Maprs148579886
PheGenIrs148579886
hapmaprs148579886
1000 genomesrs148579886
hgdprs148579886
ensemblrs148579886
gopubmedrs148579886
geneviewrs148579886
scholarrs148579886
googlers148579886
pharmgkbrs148579886
gwascentralrs148579886
openSNPrs148579886
23andMers148579886
23andMe allrs148579886
SNP Nexus

SNPshotrs148579886
SNPdbers148579886
MSV3drs148579886
GWAS Ctlgrs148579886
Max Magnitude0
ClinVar
Risk rs148579886(A;A)
Alt rs148579886(A;A)
Reference rs148579886(G;G)
Significance Probable-non-pathogenic
Disease Molybdenum cofactor deficiency
Variation info
Gene MOCS1
CLNDBN Molybdenum cofactor deficiency, complementation group A
Reversed 0
HGVS NC_000006.11:g.39877666G>A
CLNSRC
CLNACC RCV000190510.2,