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rs727504064

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504064(A;A)
Make rs727504064(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position31801768
GenePAX6
is asnp
is mentioned by
dbSNPrs727504064
ebirs727504064
HLIrs727504064
Exacrs727504064
Varsomers727504064
Maprs727504064
PheGenIrs727504064
hapmaprs727504064
1000 genomesrs727504064
hgdprs727504064
ensemblrs727504064
gopubmedrs727504064
geneviewrs727504064
scholarrs727504064
googlers727504064
pharmgkbrs727504064
gwascentralrs727504064
openSNPrs727504064
23andMers727504064
23andMe allrs727504064
SNP Nexus

SNPshotrs727504064
SNPdbers727504064
MSV3drs727504064
GWAS Ctlgrs727504064
Max Magnitude0
ClinVar
Risk rs727504064(A,T;A,T)
Alt rs727504064(A,T;A,T)
Reference rs727504064(C;C)
Significance Pathogenic
Disease not provided Anophthalmia - microphthalmia
Variation info
Gene PAX6
CLNDBN not provided Anophthalmia - microphthalmia
Reversed 1
HGVS NC_000011.9:g.31823316G>T
CLNSRC
CLNACC RCV000153641.3, RCV000207422.1,