rs387906519

Orientation

minus

Stabilized

minus

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

Make rs387906519(CCTC;GA)

Make rs387906519(GA;GA)

Reference

GRCh38 38.1/141

Chromosome

6

Position

49636656

Gene

RHAG

is a	snp
is	mentioned by
dbSNP	rs387906519
dbSNP (classic)	rs387906519
ClinGen	rs387906519
ebi	rs387906519
HLI	rs387906519
Exac	rs387906519
Gnomad	rs387906519
Varsome	rs387906519
LitVar	rs387906519
Map	rs387906519
PheGenI	rs387906519
Biobank	rs387906519
1000 genomes	rs387906519
hgdp	rs387906519
ensembl	rs387906519
geneview	rs387906519
scholar	rs387906519
google	rs387906519
pharmgkb	rs387906519
gwascentral	rs387906519
openSNP	rs387906519
23andMe	rs387906519
SNPshot	rs387906519
SNPdbe	rs387906519
MSV3d	rs387906519
GWAS Ctlg	rs387906519

Max Magnitude

0

ClinVar
Risk	rs387906519(GA;GA)
Alt	rs387906519(GA;GA)
Reference	Rs387906519(CCTC;CCTC)
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.49604369_49604372delGAGGinsTC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013932.25,