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

rs398122797

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs398122797(-;-)
Make rs398122797(-;TT)
ReferenceGRCh38 38.1/141
Chromosome5
Position53098629
GeneMOCS2
is asnp
is mentioned by
dbSNPrs398122797
ebirs398122797
HLIrs398122797
Exacrs398122797
Varsomers398122797
Maprs398122797
PheGenIrs398122797
hapmaprs398122797
1000 genomesrs398122797
hgdprs398122797
ensemblrs398122797
gopubmedrs398122797
geneviewrs398122797
scholarrs398122797
googlers398122797
pharmgkbrs398122797
gwascentralrs398122797
openSNPrs398122797
23andMers398122797
23andMe allrs398122797
SNP Nexus

SNPshotrs398122797
SNPdbers398122797
MSV3drs398122797
GWAS Ctlgrs398122797
Max Magnitude0
ClinVar
Risk rs398122797(;)
Alt rs398122797(;)
Reference rs398122797(TT;TT)
Significance Other
Disease Molybdenum cofactor deficiency
Variation info
Gene MOCS2
CLNDBN Molybdenum cofactor deficiency, complementation group B
Reversed 0
HGVS NC_000005.9:g.52394459_52394460delTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000006482.3,