rs377147994

Orientation

plus

Stabilized

plus

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

Make rs377147994(A;A)

Make rs377147994(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

40411354

Gene

IVD

is a	snp
is	mentioned by
dbSNP	rs377147994
dbSNP (classic)	rs377147994
ClinGen	rs377147994
ebi	rs377147994
HLI	rs377147994
Exac	rs377147994
Gnomad	rs377147994
Varsome	rs377147994
LitVar	rs377147994
Map	rs377147994
PheGenI	rs377147994
Biobank	rs377147994
1000 genomes	rs377147994
hgdp	rs377147994
ensembl	rs377147994
geneview	rs377147994
scholar	rs377147994
google	rs377147994
pharmgkb	rs377147994
gwascentral	rs377147994
openSNP	rs377147994
23andMe	rs377147994
SNPshot	rs377147994
SNPdbe	rs377147994
MSV3d	rs377147994
GWAS Ctlg	rs377147994

Max Magnitude

0

ClinVar
Risk	rs377147994(A;A)
Alt	rs377147994(A;A)
Reference	Rs377147994(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	IVD
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.40703553G>A
CLNSRC
CLNACC	RCV000413513.1,