rs371610471

Orientation

plus

Stabilized

plus

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

Make rs371610471(C;T)

Make rs371610471(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

136327158

Gene

PCCB

is a	snp
is	mentioned by
dbSNP	rs371610471
dbSNP (classic)	rs371610471
ClinGen	rs371610471
ebi	rs371610471
HLI	rs371610471
Exac	rs371610471
Gnomad	rs371610471
Varsome	rs371610471
LitVar	rs371610471
Map	rs371610471
PheGenI	rs371610471
Biobank	rs371610471
1000 genomes	rs371610471
hgdp	rs371610471
ensembl	rs371610471
geneview	rs371610471
scholar	rs371610471
google	rs371610471
pharmgkb	rs371610471
gwascentral	rs371610471
openSNP	rs371610471
23andMe	rs371610471
SNPshot	rs371610471
SNPdbe	rs371610471
MSV3d	rs371610471
GWAS Ctlg	rs371610471

Max Magnitude

0

ClinVar
Risk	rs371610471(T;T)
Alt	rs371610471(T;T)
Reference	Rs371610471(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCCB
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.136046000C>A
CLNSRC
CLNACC	RCV000186090.1,