rs267606900

Orientation

minus

Stabilized

minus

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

Make rs267606900(A;G)

Make rs267606900(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

30313926

Gene

MTPAP

is a	snp
is	mentioned by
dbSNP	rs267606900
dbSNP (classic)	rs267606900
ClinGen	rs267606900
ebi	rs267606900
HLI	rs267606900
Exac	rs267606900
Gnomad	rs267606900
Varsome	rs267606900
LitVar	rs267606900
Map	rs267606900
PheGenI	rs267606900
Biobank	rs267606900
1000 genomes	rs267606900
hgdp	rs267606900
ensembl	rs267606900
geneview	rs267606900
scholar	rs267606900
google	rs267606900
pharmgkb	rs267606900
gwascentral	rs267606900
openSNP	rs267606900
23andMe	rs267606900
SNPshot	rs267606900
SNPdbe	rs267606900
MSV3d	rs267606900
GWAS Ctlg	rs267606900

Max Magnitude

0

ClinVar
Risk	rs267606900(G;G)
Alt	rs267606900(G;G)
Reference	Rs267606900(A;A)
Significance	Pathogenic
Disease	Ataxia
Variation	info
Gene	MTPAP
CLNDBN	Ataxia, spastic, 4, autosomal recessive
Reversed	1
HGVS	NC_000010.10:g.30602855T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000000002.3,