rs104894669

Orientation

plus

Stabilized

plus

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

Make rs104894669(A;A)

Make rs104894669(A;G)

Reference

GRCh37 37.1/132

Chromosome

19

Position

580428

Gene

BSG

is a	snp
is	mentioned by
dbSNP	rs104894669
dbSNP (classic)	rs104894669
ClinGen	rs104894669
ebi	rs104894669
HLI	rs104894669
Exac	rs104894669
Gnomad	rs104894669
Varsome	rs104894669
LitVar	rs104894669
Map	rs104894669
PheGenI	rs104894669
Biobank	rs104894669
1000 genomes	rs104894669
hgdp	rs104894669
ensembl	rs104894669
geneview	rs104894669
scholar	rs104894669
google	rs104894669
pharmgkb	rs104894669
gwascentral	rs104894669
openSNP	rs104894669
23andMe	rs104894669
SNPshot	rs104894669
SNPdbe	rs104894669
MSV3d	rs104894669
GWAS Ctlg	rs104894669

Max Magnitude

0

OMIM	109480
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894669(A;A)
Alt	rs104894669(A;A)
Reference	Rs104894669(G;G)
Significance	Other
Disease	BLOOD GROUP--OK
Variation	info
Gene	BSG
CLNDBN	BLOOD GROUP--OK
Reversed	0
HGVS	NC_000019.9:g.580428G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019327.24,