rs267606794

Orientation

minus

Stabilized

minus

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

Make rs267606794(C;T)

Make rs267606794(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

61840319

Gene

FAM161A

is a	snp
is	mentioned by
dbSNP	rs267606794
dbSNP (classic)	rs267606794
ClinGen	rs267606794
ebi	rs267606794
HLI	rs267606794
Exac	rs267606794
Gnomad	rs267606794
Varsome	rs267606794
LitVar	rs267606794
Map	rs267606794
PheGenI	rs267606794
Biobank	rs267606794
1000 genomes	rs267606794
hgdp	rs267606794
ensembl	rs267606794
geneview	rs267606794
scholar	rs267606794
google	rs267606794
pharmgkb	rs267606794
gwascentral	rs267606794
openSNP	rs267606794
23andMe	rs267606794
SNPshot	rs267606794
SNPdbe	rs267606794
MSV3d	rs267606794
GWAS Ctlg	rs267606794

Max Magnitude

0

ClinVar
Risk	rs267606794(T;T)
Alt	rs267606794(T;T)
Reference	Rs267606794(C;C)
Significance	Pathogenic
Disease	Retinitis pigmentosa 28
Variation	info
Gene	FAM161A
CLNDBN	Retinitis pigmentosa 28
Reversed	1
HGVS	NC_000002.11:g.62067454G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000052.2,