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rs202193201

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202193201(A;A)
Make rs202193201(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position61839437
GeneFAM161A
is asnp
is mentioned by
dbSNPrs202193201
ebirs202193201
HLIrs202193201
Exacrs202193201
Varsomers202193201
Maprs202193201
PheGenIrs202193201
hapmaprs202193201
1000 genomesrs202193201
hgdprs202193201
ensemblrs202193201
gopubmedrs202193201
geneviewrs202193201
scholarrs202193201
googlers202193201
pharmgkbrs202193201
gwascentralrs202193201
openSNPrs202193201
23andMers202193201
23andMe allrs202193201
SNP Nexus

SNPshotrs202193201
SNPdbers202193201
MSV3drs202193201
GWAS Ctlgrs202193201
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs202193201(A,C,T;A,C,T)
Alt rs202193201(A,C,T;A,C,T)
Reference rs202193201(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 28 not provided
Variation info
Gene FAM161A
CLNDBN Retinitis pigmentosa 28 not provided
Reversed 0
HGVS NC_000002.11:g.62066572G>A
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000000055.2, RCV000153224.2,