rs878853341

Orientation

plus

Stabilized

plus

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

Make rs878853341(-;-)

Make rs878853341(-;GAGGCTCCAAGGTAAGTCTGGAGAAAGAGGA)

Make rs878853341(GAGGCTCCAAGGTAAGTCTGGAGAAAGAGGA;GAGGCTCCAAGGTAAGTCTGGAGAAAGAGGA)

Reference

GRCh38.p2 38.2/147

Chromosome

14

Position

67727180

Gene	GPHN, RDH12

is a	snp
is	mentioned by
dbSNP	rs878853341
dbSNP (classic)	rs878853341
ClinGen	rs878853341
ebi	rs878853341
HLI	rs878853341
Exac	rs878853341
Gnomad	rs878853341
Varsome	rs878853341
LitVar	rs878853341
Map	rs878853341
PheGenI	rs878853341
Biobank	rs878853341
1000 genomes	rs878853341
hgdp	rs878853341
ensembl	rs878853341
geneview	rs878853341
scholar	rs878853341
google	rs878853341
pharmgkb	rs878853341
gwascentral	rs878853341
openSNP	rs878853341
23andMe	rs878853341
SNPshot	rs878853341
SNPdbe	rs878853341
MSV3d	rs878853341
GWAS Ctlg	rs878853341

Max Magnitude

0

ClinVar
Risk	rs878853341(-;-)
Alt	rs878853341(-;-)
Reference	Rs878853341(AGAGGCTCCAAGGTAAGTCTGGAGAAAGAGG;AGAGGCTCCAAGGTAAGTCTGGAGAAAGAGG)
Significance	Probable-Pathogenic
Disease	Retinal dystrophy
Variation	info
Gene	RDH12
CLNDBN	Retinal dystrophy
Reversed	0
HGVS	NC_000014.8:g.68193897_68193927del31
CLNSRC
CLNACC	RCV000225678.1,