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rs749909863

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs749909863(C;T)
Make rs749909863(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position64230600
GeneEYS
is asnp
is mentioned by
dbSNPrs749909863
ebirs749909863
HLIrs749909863
Exacrs749909863
Varsomers749909863
Maprs749909863
PheGenIrs749909863
hapmaprs749909863
1000 genomesrs749909863
hgdprs749909863
ensemblrs749909863
gopubmedrs749909863
geneviewrs749909863
scholarrs749909863
googlers749909863
pharmgkbrs749909863
gwascentralrs749909863
openSNPrs749909863
23andMers749909863
23andMe allrs749909863
SNP Nexus

SNPshotrs749909863
SNPdbers749909863
MSV3drs749909863
GWAS Ctlgrs749909863
Max Magnitude0
ClinVar
Risk rs749909863(T;T)
Alt rs749909863(T;T)
Reference rs749909863(C;C)
Significance Pathogenic
Disease not specified Retinitis pigmentosa 25
Variation info
Gene EYS
CLNDBN not specified Retinitis pigmentosa 25
Reversed 0
HGVS NC_000006.11:g.64940493C>T
CLNSRC
CLNACC RCV000169660.1, RCV000177524.1,