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rs387907276

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907276(A;A)
Make rs387907276(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position44313931
GeneSLC3A1
is asnp
is mentioned by
dbSNPrs387907276
dbSNP (classic)rs387907276
ClinGenrs387907276
ebirs387907276
HLIrs387907276
Exacrs387907276
Gnomadrs387907276
Varsomers387907276
LitVarrs387907276
Maprs387907276
PheGenIrs387907276
Biobankrs387907276
1000 genomesrs387907276
hgdprs387907276
ensemblrs387907276
geneviewrs387907276
scholarrs387907276
googlers387907276
pharmgkbrs387907276
gwascentralrs387907276
openSNPrs387907276
23andMers387907276
SNPshotrs387907276
SNPdbers387907276
MSV3drs387907276
GWAS Ctlgrs387907276
Max Magnitude0
ClinVar
Risk rs387907276(A;A) rs387907276(G;G)
Alt rs387907276(A;A) rs387907276(G;G)
Reference Rs387907276(T;T)
Significance Pathogenic
Disease Cystinuria
Variation info
Gene SLC3A1
CLNDBN Cystinuria
Reversed 0
HGVS NC_000002.11:g.44541070T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030727.27,