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rs1064797180

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome13
Position110439788
GeneCOL4A2
is asnp
is mentioned by
dbSNPrs1064797180
dbSNP (classic)rs1064797180
ClinGenrs1064797180
ebirs1064797180
HLIrs1064797180
Exacrs1064797180
Gnomadrs1064797180
Varsomers1064797180
LitVarrs1064797180
Maprs1064797180
PheGenIrs1064797180
Biobankrs1064797180
1000 genomesrs1064797180
hgdprs1064797180
ensemblrs1064797180
geneviewrs1064797180
scholarrs1064797180
googlers1064797180
pharmgkbrs1064797180
gwascentralrs1064797180
openSNPrs1064797180
23andMers1064797180
23andMe allrs1064797180
SNPshotrs1064797180
SNPdbers1064797180
MSV3drs1064797180
GWAS Ctlgrs1064797180
Max Magnitude0
ClinVar
Risk rs1064797180(A;A)
Alt rs1064797180(A;A)
Reference Rs1064797180(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL4A2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.111092135G>A
CLNSRC
CLNACC RCV000487860.1,