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rs374664941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374664941(C;T)
Make rs374664941(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position15644210
GeneITGA8
is asnp
is mentioned by
dbSNPrs374664941
ebirs374664941
HLIrs374664941
Exacrs374664941
Varsomers374664941
Maprs374664941
PheGenIrs374664941
hapmaprs374664941
1000 genomesrs374664941
hgdprs374664941
ensemblrs374664941
gopubmedrs374664941
geneviewrs374664941
scholarrs374664941
googlers374664941
pharmgkbrs374664941
gwascentralrs374664941
openSNPrs374664941
23andMers374664941
23andMe allrs374664941
SNP Nexus

SNPshotrs374664941
SNPdbers374664941
MSV3drs374664941
GWAS Ctlgrs374664941
Max Magnitude0
ClinVar
Risk rs374664941(T;T)
Alt rs374664941(T;T)
Reference rs374664941(C;C)
Significance Pathogenic
Disease Renal adysplasia
Variation info
Gene ITGA8
CLNDBN Renal adysplasia
Reversed 0
HGVS NC_000010.10:g.15686209C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000114395.3,