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rs121908606

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908606(A;A)
Make rs121908606(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position53107172
GeneMOCS2
is asnp
is mentioned by
dbSNPrs121908606
ebirs121908606
HLIrs121908606
Exacrs121908606
Varsomers121908606
Maprs121908606
PheGenIrs121908606
hapmaprs121908606
1000 genomesrs121908606
hgdprs121908606
ensemblrs121908606
gopubmedrs121908606
geneviewrs121908606
scholarrs121908606
googlers121908606
pharmgkbrs121908606
gwascentralrs121908606
openSNPrs121908606
23andMers121908606
23andMe allrs121908606
SNP Nexus

SNPshotrs121908606
SNPdbers121908606
MSV3drs121908606
GWAS Ctlgrs121908606
Max Magnitude0
OMIM603708
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121908606(A;A)
Alt rs121908606(A;A)
Reference rs121908606(G;G)
Significance Pathogenic
Disease Molybdenum cofactor deficiency
Variation info
Gene MOCS2
CLNDBN Molybdenum cofactor deficiency, complementation group B
Reversed 1
HGVS NC_000005.9:g.52403002C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006486.3,