rs587777100

Orientation

plus

Stabilized

plus

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

Make rs587777100(A;A)

Make rs587777100(A;T)

Reference

GRCh38 38.1/142

Chromosome

15

Position

36697379

Gene

C15orf41

is a	snp
is	mentioned by
dbSNP	rs587777100
dbSNP (classic)	rs587777100
ClinGen	rs587777100
ebi	rs587777100
HLI	rs587777100
Exac	rs587777100
Gnomad	rs587777100
Varsome	rs587777100
LitVar	rs587777100
Map	rs587777100
PheGenI	rs587777100
Biobank	rs587777100
1000 genomes	rs587777100
hgdp	rs587777100
ensembl	rs587777100
geneview	rs587777100
scholar	rs587777100
google	rs587777100
pharmgkb	rs587777100
gwascentral	rs587777100
openSNP	rs587777100
23andMe	rs587777100
SNPshot	rs587777100
SNPdbe	rs587777100
MSV3d	rs587777100
GWAS Ctlg	rs587777100

Max Magnitude

0

ClinVar
Risk	rs587777100(A;A)
Alt	rs587777100(A;A)
Reference	Rs587777100(T;T)
Significance	Pathogenic
Disease	ANEMIA
Variation	info
Gene	C15orf41
CLNDBN	ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib
Reversed	0
HGVS	NC_000015.9:g.36989580T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000083301.4,