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rs769211787

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs769211787(A;C)
Make rs769211787(C;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position108157002
GeneCOL4A6
is asnp
is mentioned by
dbSNPrs769211787
ebirs769211787
HLIrs769211787
Exacrs769211787
Varsomers769211787
Maprs769211787
PheGenIrs769211787
hapmaprs769211787
1000 genomesrs769211787
hgdprs769211787
ensemblrs769211787
gopubmedrs769211787
geneviewrs769211787
scholarrs769211787
googlers769211787
pharmgkbrs769211787
gwascentralrs769211787
openSNPrs769211787
23andMers769211787
23andMe allrs769211787
SNP Nexus

SNPshotrs769211787
SNPdbers769211787
MSV3drs769211787
GWAS Ctlgrs769211787
Max Magnitude0
ClinVar
Risk rs769211787(C;C)
Alt rs769211787(C;C)
Reference rs769211787(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL4A6
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.107400232A>C
CLNSRC
CLNACC RCV000171443.1,