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rs780085174

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs780085174(C;T)
Make rs780085174(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position53102097
GeneMOCS2
is asnp
is mentioned by
dbSNPrs780085174
dbSNP (classic)rs780085174
ClinGenrs780085174
ebirs780085174
HLIrs780085174
Exacrs780085174
Gnomadrs780085174
Varsomers780085174
LitVarrs780085174
Maprs780085174
PheGenIrs780085174
Biobankrs780085174
1000 genomesrs780085174
hgdprs780085174
ensemblrs780085174
geneviewrs780085174
scholarrs780085174
googlers780085174
pharmgkbrs780085174
gwascentralrs780085174
openSNPrs780085174
23andMers780085174
23andMe allrs780085174
SNPshotrs780085174
SNPdbers780085174
MSV3drs780085174
GWAS Ctlgrs780085174
Max Magnitude0
ClinVar
Risk rs780085174(T;T)
Alt rs780085174(T;T)
Reference Rs780085174(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MOCS2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.52397927C>T
CLNSRC
CLNACC RCV000479116.1,