rs786205858

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs786205858(A;A)

Make rs786205858(A;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

27457760

Gene

IFT172

is a	snp
is	mentioned by
dbSNP	rs786205858
dbSNP (classic)	rs786205858
ClinGen	rs786205858
ebi	rs786205858
HLI	rs786205858
Exac	rs786205858
Gnomad	rs786205858
Varsome	rs786205858
LitVar	rs786205858
Map	rs786205858
PheGenI	rs786205858
Biobank	rs786205858
1000 genomes	rs786205858
hgdp	rs786205858
ensembl	rs786205858
geneview	rs786205858
scholar	rs786205858
google	rs786205858
pharmgkb	rs786205858
gwascentral	rs786205858
openSNP	rs786205858
23andMe	rs786205858
SNPshot	rs786205858
SNPdbe	rs786205858
MSV3d	rs786205858
GWAS Ctlg	rs786205858

Max Magnitude

0

ClinVar
Risk	rs786205858(A;A)
Alt	rs786205858(A;A)
Reference	Rs786205858(T;T)
Significance	Pathogenic
Disease	Retinitis pigmentosa 71
Variation	info
Gene	IFT172
CLNDBN	Retinitis pigmentosa 71
Reversed	1
HGVS	NC_000002.11:g.27680627A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000171552.2,