rs121918133

Orientation

plus

Stabilized

plus

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

Make rs121918133(C;T)

Make rs121918133(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44812319

Gene

BCAM

is a	snp
is	mentioned by
dbSNP	rs121918133
dbSNP (classic)	rs121918133
ClinGen	rs121918133
ebi	rs121918133
HLI	rs121918133
Exac	rs121918133
Gnomad	rs121918133
Varsome	rs121918133
LitVar	rs121918133
Map	rs121918133
PheGenI	rs121918133
Biobank	rs121918133
1000 genomes	rs121918133
hgdp	rs121918133
ensembl	rs121918133
geneview	rs121918133
scholar	rs121918133
google	rs121918133
pharmgkb	rs121918133
gwascentral	rs121918133
openSNP	rs121918133
23andMe	rs121918133
SNPshot	rs121918133
SNPdbe	rs121918133
MSV3d	rs121918133
GWAS Ctlg	rs121918133

Max Magnitude

0

OMIM	612773
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121918133(T;T)
Alt	rs121918133(T;T)
Reference	Rs121918133(C;C)
Significance	Pathogenic
Disease	BLOOD GROUP--LUTHERAN NULL
Variation	info
Gene	BCAM
CLNDBN	BLOOD GROUP--LUTHERAN NULL
Reversed	0
HGVS	NC_000019.9:g.45315576C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000472.1,