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rs387906735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906735(A;G)
Make rs387906735(G;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position608
GeneGTF2IRD1
is asnp
is mentioned by
dbSNPrs387906735
ebirs387906735
HLIrs387906735
Exacrs387906735
Varsomers387906735
Maprs387906735
PheGenIrs387906735
hapmaprs387906735
1000 genomesrs387906735
hgdprs387906735
ensemblrs387906735
gopubmedrs387906735
geneviewrs387906735
scholarrs387906735
googlers387906735
pharmgkbrs387906735
gwascentralrs387906735
openSNPrs387906735
23andMers387906735
23andMe allrs387906735
SNP Nexus

SNPshotrs387906735
SNPdbers387906735
MSV3drs387906735
GWAS Ctlgrs387906735
Max Magnitude0
ClinVar
Risk rs387906735(G;G)
Alt rs387906735(G;G)
Reference rs387906735(A;A)
Significance Pathogenic
Disease Nephropathy
Variation info
Gene
CLNDBN Nephropathy, tubulointerstitial
Reversed 0
HGVS NC_012920.1:m.608A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022904.4,