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rs786205896

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205896(A;G)
Make rs786205896(G;G)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position132085670
GeneFRMD7
is asnp
is mentioned by
dbSNPrs786205896
ebirs786205896
HLIrs786205896
Exacrs786205896
Varsomers786205896
Maprs786205896
PheGenIrs786205896
hapmaprs786205896
1000 genomesrs786205896
hgdprs786205896
ensemblrs786205896
gopubmedrs786205896
geneviewrs786205896
scholarrs786205896
googlers786205896
pharmgkbrs786205896
gwascentralrs786205896
openSNPrs786205896
23andMers786205896
23andMe allrs786205896
SNP Nexus

SNPshotrs786205896
SNPdbers786205896
MSV3drs786205896
GWAS Ctlgrs786205896
Max Magnitude0
ClinVar
Risk rs786205896(G;G)
Alt rs786205896(G;G)
Reference rs786205896(A;A)
Significance Pathogenic
Disease Infantile nystagmus
Variation info
Gene FRMD7
CLNDBN Infantile nystagmus, X-linked
Reversed 1
HGVS NC_000023.10:g.131219698T>C
CLNSRC
CLNACC RCV000172871.1,