rs104893987

Orientation

minus

Stabilized

minus

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

Make rs104893987(A;A)

Make rs104893987(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

49612504

Gene

RHAG

is a	snp
is	mentioned by
dbSNP	rs104893987
dbSNP (classic)	rs104893987
ClinGen	rs104893987
ebi	rs104893987
HLI	rs104893987
Exac	rs104893987
Gnomad	rs104893987
Varsome	rs104893987
LitVar	rs104893987
Map	rs104893987
PheGenI	rs104893987
Biobank	rs104893987
1000 genomes	rs104893987
hgdp	rs104893987
ensembl	rs104893987
geneview	rs104893987
scholar	rs104893987
google	rs104893987
pharmgkb	rs104893987
gwascentral	rs104893987
openSNP	rs104893987
23andMe	rs104893987
SNPshot	rs104893987
SNPdbe	rs104893987
MSV3d	rs104893987
GWAS Ctlg	rs104893987

Max Magnitude

0

OMIM	180297
Desc
Variant	0009
Related	also

ClinVar
Risk	rs104893987(A;A)
Alt	rs104893987(A;A)
Reference	Rs104893987(G;G)
Significance	Pathogenic
Disease	Rh-null hemolytic anemia
Variation	info
Gene	RHAG
CLNDBN	Rh-null hemolytic anemia, regulator type
Reversed	1
HGVS	NC_000006.11:g.49580217C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013940.25,