rs786205579

Orientation

minus

Stabilized

minus

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

Make rs786205579(A;A)

Make rs786205579(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

42721838

Gene

PRPH2

is a	snp
is	mentioned by
dbSNP	rs786205579
dbSNP (classic)	rs786205579
ClinGen	rs786205579
ebi	rs786205579
HLI	rs786205579
Exac	rs786205579
Gnomad	rs786205579
Varsome	rs786205579
LitVar	rs786205579
Map	rs786205579
PheGenI	rs786205579
Biobank	rs786205579
1000 genomes	rs786205579
hgdp	rs786205579
ensembl	rs786205579
geneview	rs786205579
scholar	rs786205579
google	rs786205579
pharmgkb	rs786205579
gwascentral	rs786205579
openSNP	rs786205579
23andMe	rs786205579
SNPshot	rs786205579
SNPdbe	rs786205579
MSV3d	rs786205579
GWAS Ctlg	rs786205579

Max Magnitude

0

ClinVar
Risk	rs786205579(A;A)
Alt	rs786205579(A;A)
Reference	Rs786205579(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PRPH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000006.11:g.42689576C>T
CLNSRC
CLNACC	RCV000171395.1,