rs138211175

Orientation

plus

Stabilized

plus

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

Make rs138211175(C;T)

Make rs138211175(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

21

Position

43058919

Gene

CBS

is a	snp
is	mentioned by
dbSNP	rs138211175
dbSNP (classic)	rs138211175
ClinGen	rs138211175
ebi	rs138211175
HLI	rs138211175
Exac	rs138211175
Gnomad	rs138211175
Varsome	rs138211175
LitVar	rs138211175
Map	rs138211175
PheGenI	rs138211175
Biobank	rs138211175
1000 genomes	rs138211175
hgdp	rs138211175
ensembl	rs138211175
geneview	rs138211175
scholar	rs138211175
google	rs138211175
pharmgkb	rs138211175
gwascentral	rs138211175
openSNP	rs138211175
23andMe	rs138211175
SNPshot	rs138211175
SNPdbe	rs138211175
MSV3d	rs138211175
GWAS Ctlg	rs138211175

Max Magnitude

0

ClinVar
Risk	rs138211175(T;T)
Alt	rs138211175(T;T)
Reference	Rs138211175(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CBS
CLNDBN	not provided
Reversed	0
HGVS	NC_000021.8:g.44479029C>T
CLNSRC
CLNACC	RCV000200590.1,