rs121918132

Orientation

plus

Stabilized

plus

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

Make rs121918132(C;T)

Make rs121918132(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44813527

Gene

BCAM

is a	snp
is	mentioned by
dbSNP	rs121918132
dbSNP (classic)	rs121918132
ClinGen	rs121918132
ebi	rs121918132
HLI	rs121918132
Exac	rs121918132
Gnomad	rs121918132
Varsome	rs121918132
LitVar	rs121918132
Map	rs121918132
PheGenI	rs121918132
Biobank	rs121918132
1000 genomes	rs121918132
hgdp	rs121918132
ensembl	rs121918132
geneview	rs121918132
scholar	rs121918132
google	rs121918132
pharmgkb	rs121918132
gwascentral	rs121918132
openSNP	rs121918132
23andMe	rs121918132
SNPshot	rs121918132
SNPdbe	rs121918132
MSV3d	rs121918132
GWAS Ctlg	rs121918132

Max Magnitude

0

OMIM	612773
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121918132(T;T)
Alt	rs121918132(T;T)
Reference	Rs121918132(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.45316784C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000469.2,