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rs370540673

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370540673(C;T)
Make rs370540673(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position27471096
GeneIFT172
is asnp
is mentioned by
dbSNPrs370540673
ebirs370540673
HLIrs370540673
Exacrs370540673
Varsomers370540673
Maprs370540673
PheGenIrs370540673
hapmaprs370540673
1000 genomesrs370540673
hgdprs370540673
ensemblrs370540673
gopubmedrs370540673
geneviewrs370540673
scholarrs370540673
googlers370540673
pharmgkbrs370540673
gwascentralrs370540673
openSNPrs370540673
23andMers370540673
23andMe allrs370540673
SNP Nexus

SNPshotrs370540673
SNPdbers370540673
MSV3drs370540673
GWAS Ctlgrs370540673
Max Magnitude0
ClinVar
Risk rs370540673(A,T;A,T)
Alt rs370540673(A,T;A,T)
Reference rs370540673(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 71
Variation info
Gene IFT172
CLNDBN Retinitis pigmentosa 71
Reversed 0
HGVS NC_000002.11:g.27693963C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000171549.2,