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rs77010315

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs77010315(A;A)
Make rs77010315(A;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position151343594
GeneSLC36A2
is asnp
is mentioned by
dbSNPrs77010315
ebirs77010315
HLIrs77010315
Exacrs77010315
Varsomers77010315
Maprs77010315
PheGenIrs77010315
hapmaprs77010315
1000 genomesrs77010315
hgdprs77010315
ensemblrs77010315
gopubmedrs77010315
geneviewrs77010315
scholarrs77010315
googlers77010315
pharmgkbrs77010315
gwascentralrs77010315
openSNPrs77010315
23andMers77010315
23andMe allrs77010315
SNP Nexus

SNPshotrs77010315
SNPdbers77010315
MSV3drs77010315
GWAS Ctlgrs77010315
GMAF0.007346
Max Magnitude0
ClinVar
Risk rs77010315(A;A)
Alt rs77010315(A;A)
Reference rs77010315(C;C)
Significance Pathogenic
Disease Iminoglycinuria Hyperglycinuria
Variation info
Gene SLC36A2
CLNDBN Iminoglycinuria, digenic Hyperglycinuria
Reversed 0
HGVS NC_000005.9:g.150723155C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002483.2, RCV000002484.2,