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rs786205856

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205856(G;G)
Make rs786205856(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position27445929
GeneIFT172, KRTCAP3
is asnp
is mentioned by
dbSNPrs786205856
ebirs786205856
HLIrs786205856
Exacrs786205856
Varsomers786205856
Maprs786205856
PheGenIrs786205856
hapmaprs786205856
1000 genomesrs786205856
hgdprs786205856
ensemblrs786205856
gopubmedrs786205856
geneviewrs786205856
scholarrs786205856
googlers786205856
pharmgkbrs786205856
gwascentralrs786205856
openSNPrs786205856
23andMers786205856
23andMe allrs786205856
SNP Nexus

SNPshotrs786205856
SNPdbers786205856
MSV3drs786205856
GWAS Ctlgrs786205856
Max Magnitude0
ClinVar
Risk rs786205856(G;G)
Alt rs786205856(G;G)
Reference rs786205856(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 71
Variation info
Gene KRTCAP3 IFT172
CLNDBN Retinitis pigmentosa 71
Reversed 1
HGVS NC_000002.11:g.27668796A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000171550.2,