rs387906265

Orientation

plus

Stabilized

plus

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

Make rs387906265(-;-)

Make rs387906265(-;GA)

Reference

GRCh38 38.1/141

Chromosome

1

Position

42830989

Gene

ERMAP

is a	snp
is	mentioned by
dbSNP	rs387906265
dbSNP (classic)	rs387906265
ClinGen	rs387906265
ebi	rs387906265
HLI	rs387906265
Exac	rs387906265
Gnomad	rs387906265
Varsome	rs387906265
LitVar	rs387906265
Map	rs387906265
PheGenI	rs387906265
Biobank	rs387906265
1000 genomes	rs387906265
hgdp	rs387906265
ensembl	rs387906265
geneview	rs387906265
scholar	rs387906265
google	rs387906265
pharmgkb	rs387906265
gwascentral	rs387906265
openSNP	rs387906265
23andMe	rs387906265
SNPshot	rs387906265
SNPdbe	rs387906265
MSV3d	rs387906265
GWAS Ctlg	rs387906265

Max Magnitude

0

ClinVar
Risk	rs387906265(-;-)
Alt	rs387906265(-;-)
Reference	Rs387906265(GA;GA)
Significance	Pathogenic
Disease	SCIANNA BLOOD GROUP SYSTEM
Variation	info
Gene	ERMAP
CLNDBN	SCIANNA BLOOD GROUP SYSTEM, SC:-1,-2
Reversed	0
HGVS	NC_000001.10:g.43296660_43296661delGA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001992.3,