rs104894130

Orientation

plus

Stabilized

plus

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

Make rs104894130(C;G)

Make rs104894130(G;G)

Reference

GRCh37 37.1/132

Chromosome

9

Position

12695626

Gene

TYRP1

is a	snp
is	mentioned by
dbSNP	rs104894130
dbSNP (classic)	rs104894130
ClinGen	rs104894130
ebi	rs104894130
HLI	rs104894130
Exac	rs104894130
Gnomad	rs104894130
Varsome	rs104894130
LitVar	rs104894130
Map	rs104894130
PheGenI	rs104894130
Biobank	rs104894130
1000 genomes	rs104894130
hgdp	rs104894130
ensembl	rs104894130
geneview	rs104894130
scholar	rs104894130
google	rs104894130
pharmgkb	rs104894130
gwascentral	rs104894130
openSNP	rs104894130
23andMe	rs104894130
SNPshot	rs104894130
SNPdbe	rs104894130
MSV3d	rs104894130
GWAS Ctlg	rs104894130

Max Magnitude

0

OMIM	115501
Desc
Variant	0002
Related	also

ClinVar
Risk	rs104894130(G;G)
Alt	rs104894130(G;G)
Reference	Rs104894130(C;C)
Significance	Other
Disease	Oculocutaneous albinism type 3 OCULOCUTANEOUS ALBINISM not provided
Variation	info
Gene	TYRP1
CLNDBN	Oculocutaneous albinism type 3 OCULOCUTANEOUS ALBINISM, TYPE II, MODIFIER OF not provided
Reversed	0
HGVS	NC_000009.11:g.12695626C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019159.25, RCV000019160.26, RCV000373290.1,