rs121918587

Orientation

minus

Stabilized

minus

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

Make rs121918587(A;A)

Make rs121918587(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

49612506

Gene

RHAG

is a	snp
is	mentioned by
dbSNP	rs121918587
dbSNP (classic)	rs121918587
ClinGen	rs121918587
ebi	rs121918587
HLI	rs121918587
Exac	rs121918587
Gnomad	rs121918587
Varsome	rs121918587
LitVar	rs121918587
Map	rs121918587
PheGenI	rs121918587
Biobank	rs121918587
1000 genomes	rs121918587
hgdp	rs121918587
ensembl	rs121918587
geneview	rs121918587
scholar	rs121918587
google	rs121918587
pharmgkb	rs121918587
gwascentral	rs121918587
openSNP	rs121918587
23andMe	rs121918587
SNPshot	rs121918587
SNPdbe	rs121918587
MSV3d	rs121918587
GWAS Ctlg	rs121918587

Merged from

Rs28933991

Max Magnitude

0

aka c.836G>A (p.Gly279Glu or G279E)

23andMe name: i5900457

OMIM	180297
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121918587(A;A)
Alt	rs121918587(A;A)
Reference	Rs121918587(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.49580219C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013935.18,