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rs786205548

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205548(A;T)
Make rs786205548(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position227033407
GeneCOL4A4
is asnp
is mentioned by
dbSNPrs786205548
ebirs786205548
HLIrs786205548
Exacrs786205548
Varsomers786205548
Maprs786205548
PheGenIrs786205548
hapmaprs786205548
1000 genomesrs786205548
hgdprs786205548
ensemblrs786205548
gopubmedrs786205548
geneviewrs786205548
scholarrs786205548
googlers786205548
pharmgkbrs786205548
gwascentralrs786205548
openSNPrs786205548
23andMers786205548
23andMe allrs786205548
SNP Nexus

SNPshotrs786205548
SNPdbers786205548
MSV3drs786205548
GWAS Ctlgrs786205548
Max Magnitude0
ClinVar
Risk rs786205548(T;T)
Alt rs786205548(T;T)
Reference rs786205548(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL4A4
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.227898123T>A
CLNSRC
CLNACC RCV000171334.1,