rs371427844

Orientation

plus

Stabilized

plus

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

Make rs371427844(C;T)

Make rs371427844(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

15

Position

40418165

Gene

IVD

is a	snp
is	mentioned by
dbSNP	rs371427844
dbSNP (classic)	rs371427844
ClinGen	rs371427844
ebi	rs371427844
HLI	rs371427844
Exac	rs371427844
Gnomad	rs371427844
Varsome	rs371427844
LitVar	rs371427844
Map	rs371427844
PheGenI	rs371427844
Biobank	rs371427844
1000 genomes	rs371427844
hgdp	rs371427844
ensembl	rs371427844
geneview	rs371427844
scholar	rs371427844
google	rs371427844
pharmgkb	rs371427844
gwascentral	rs371427844
openSNP	rs371427844
23andMe	rs371427844
SNPshot	rs371427844
SNPdbe	rs371427844
MSV3d	rs371427844
GWAS Ctlg	rs371427844

Max Magnitude

0

ClinVar
Risk	rs371427844(T;T)
Alt	rs371427844(T;T)
Reference	Rs371427844(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	IVD
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.40710364C>T
CLNSRC
CLNACC	RCV000255825.1,