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rs869025326

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025326(C;C)
Make rs869025326(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position227253640
GeneCOL4A3, LOC654841
is asnp
is mentioned by
dbSNPrs869025326
ClinGenrs869025326
ebirs869025326
HLIrs869025326
Exacrs869025326
Varsomers869025326
Maprs869025326
PheGenIrs869025326
hapmaprs869025326
1000 genomesrs869025326
hgdprs869025326
ensemblrs869025326
gopubmedrs869025326
geneviewrs869025326
scholarrs869025326
googlers869025326
pharmgkbrs869025326
gwascentralrs869025326
openSNPrs869025326
23andMers869025326
23andMe allrs869025326
SNP Nexus

SNPshotrs869025326
SNPdbers869025326
MSV3drs869025326
GWAS Ctlgrs869025326
Max Magnitude0
ClinVar
Risk rs869025326(C;C)
Alt rs869025326(C;C)
Reference Rs869025326(T;T)
Significance Pathogenic
Disease Benign familial hematuria
Variation info
Gene COL4A3 LOC654841
CLNDBN Benign familial hematuria
Reversed 0
HGVS NC_000002.11:g.228118356T>C
CLNSRC
CLNACC RCV000207993.1,