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rs913435613

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs913435613(C;C)
Make rs913435613(C;T)
Make rs913435613(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position80276381
GeneMAT1A
is asnp
is mentioned by
dbSNPrs913435613
dbSNP (classic)rs913435613
ClinGenrs913435613
ebirs913435613
HLIrs913435613
Exacrs913435613
Gnomadrs913435613
Varsomers913435613
LitVarrs913435613
Maprs913435613
PheGenIrs913435613
Biobankrs913435613
1000 genomesrs913435613
hgdprs913435613
ensemblrs913435613
geneviewrs913435613
scholarrs913435613
googlers913435613
pharmgkbrs913435613
gwascentralrs913435613
openSNPrs913435613
23andMers913435613
23andMe allrs913435613
SNPshotrs913435613
SNPdbers913435613
MSV3drs913435613
GWAS Ctlgrs913435613
Max Magnitude0
ClinVar
Risk rs913435613(A;A)
Alt rs913435613(A;A)
Reference Rs913435613(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MAT1A
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.82036137G>A
CLNSRC
CLNACC RCV000433867.1,