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rs869025327

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025327(A;A)
Make rs869025327(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position227294562
GeneCOL4A3, LOC654841
is asnp
is mentioned by
dbSNPrs869025327
ebirs869025327
HLIrs869025327
Exacrs869025327
Varsomers869025327
Maprs869025327
PheGenIrs869025327
hapmaprs869025327
1000 genomesrs869025327
hgdprs869025327
ensemblrs869025327
gopubmedrs869025327
geneviewrs869025327
scholarrs869025327
googlers869025327
pharmgkbrs869025327
gwascentralrs869025327
openSNPrs869025327
23andMers869025327
23andMe allrs869025327
SNP Nexus

SNPshotrs869025327
SNPdbers869025327
MSV3drs869025327
GWAS Ctlgrs869025327
Max Magnitude0
ClinVar
Risk rs869025327(A;A)
Alt rs869025327(A;A)
Reference rs869025327(G;G)
Significance Pathogenic
Disease Benign familial hematuria
Variation info
Gene COL4A3 LOC654841
CLNDBN Benign familial hematuria
Reversed 0
HGVS NC_000002.11:g.228159278G>A
CLNSRC
CLNACC RCV000207687.1,