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rs121908605

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908605(A;A)
Make rs121908605(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position53098667
GeneMOCS2
is asnp
is mentioned by
dbSNPrs121908605
ebirs121908605
HLIrs121908605
Exacrs121908605
Varsomers121908605
Maprs121908605
PheGenIrs121908605
hapmaprs121908605
1000 genomesrs121908605
hgdprs121908605
ensemblrs121908605
gopubmedrs121908605
geneviewrs121908605
scholarrs121908605
googlers121908605
pharmgkbrs121908605
gwascentralrs121908605
openSNPrs121908605
23andMers121908605
23andMe allrs121908605
SNP Nexus

SNPshotrs121908605
SNPdbers121908605
MSV3drs121908605
GWAS Ctlgrs121908605
Max Magnitude0
OMIM603708
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908605(A;A)
Alt rs121908605(A;A)
Reference rs121908605(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.52394497C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006483.5,