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rs77775126

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs77775126(C;T)
Make rs77775126(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position54625000
GeneRP1
is asnp
is mentioned by
dbSNPrs77775126
dbSNP (old)rs77775126
ClinGenrs77775126
ebirs77775126
HLIrs77775126
Exacrs77775126
Gnomadrs77775126
Varsomers77775126
Maprs77775126
PheGenIrs77775126
Biobankrs77775126
1000 genomesrs77775126
hgdprs77775126
ensemblrs77775126
gopubmedrs77775126
geneviewrs77775126
scholarrs77775126
googlers77775126
pharmgkbrs77775126
gwascentralrs77775126
openSNPrs77775126
23andMers77775126
23andMe allrs77775126
SNP Nexus

SNPshotrs77775126
SNPdbers77775126
MSV3drs77775126
GWAS Ctlgrs77775126
GMAF0.008264
Max Magnitude0
OMIM603937
Desc
Variant0006
Relatedalso
ClinVar
Risk rs77775126(T;T)
Alt rs77775126(T;T)
Reference Rs77775126(C;C)
Significance Other
Disease Retinitis pigmentosa 1 not specified Retinitis Pigmentosa
Variation info
Gene RP1
CLNDBN Retinitis pigmentosa 1 not specified Retinitis Pigmentosa, Dominant
Reversed 0
HGVS NC_000008.10:g.55537560C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000006334.3, RCV000178267.2, RCV000270795.1,