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rs199740930

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199740930(C;T)
Make rs199740930(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position65057613
GeneEYS
is asnp
is mentioned by
dbSNPrs199740930
dbSNP (old)rs199740930
ClinGenrs199740930
ebirs199740930
HLIrs199740930
Exacrs199740930
Gnomadrs199740930
Varsomers199740930
Maprs199740930
PheGenIrs199740930
Biobankrs199740930
1000 genomesrs199740930
hgdprs199740930
ensemblrs199740930
gopubmedrs199740930
geneviewrs199740930
scholarrs199740930
googlers199740930
pharmgkbrs199740930
gwascentralrs199740930
openSNPrs199740930
23andMers199740930
23andMe allrs199740930
SNPshotrs199740930
SNPdbers199740930
MSV3drs199740930
GWAS Ctlgrs199740930
Max Magnitude0
ClinVar
Risk rs199740930(T;T)
Alt rs199740930(T;T)
Reference Rs199740930(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EYS
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.65767506C>T
CLNSRC
CLNACC RCV000484533.2,