rs145191476

Orientation

plus

Stabilized

plus

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

Make rs145191476(A;A)

Make rs145191476(A;C)

Reference

GRCh38 38.1/141

Chromosome

1

Position

108924060

Gene

GPSM2

is a	snp
is	mentioned by
dbSNP	rs145191476
dbSNP (classic)	rs145191476
ClinGen	rs145191476
ebi	rs145191476
HLI	rs145191476
Exac	rs145191476
Gnomad	rs145191476
Varsome	rs145191476
LitVar	rs145191476
Map	rs145191476
PheGenI	rs145191476
Biobank	rs145191476
1000 genomes	rs145191476
hgdp	rs145191476
ensembl	rs145191476
geneview	rs145191476
scholar	rs145191476
google	rs145191476
pharmgkb	rs145191476
gwascentral	rs145191476
openSNP	rs145191476
23andMe	rs145191476
SNPshot	rs145191476
SNPdbe	rs145191476
MSV3d	rs145191476
GWAS Ctlg	rs145191476

Max Magnitude

0

ClinVar
Risk	rs145191476(A;A)
Alt	rs145191476(A;A)
Reference	Rs145191476(C;C)
Significance	Pathogenic
Disease	Chudley-McCullough syndrome
Variation	info
Gene	GPSM2
CLNDBN	Chudley-McCullough syndrome
Reversed	0
HGVS	NC_000001.10:g.109466682C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000029165.4,