rs371900329

Orientation

plus

Stabilized

plus

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

Make rs371900329(C;T)

Make rs371900329(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

103458291

Gene

CALHM1

is a	snp
is	mentioned by
dbSNP	rs371900329
dbSNP (classic)	rs371900329
ClinGen	rs371900329
ebi	rs371900329
HLI	rs371900329
Exac	rs371900329
Gnomad	rs371900329
Varsome	rs371900329
LitVar	rs371900329
Map	rs371900329
PheGenI	rs371900329
Biobank	rs371900329
1000 genomes	rs371900329
hgdp	rs371900329
ensembl	rs371900329
geneview	rs371900329
scholar	rs371900329
google	rs371900329
pharmgkb	rs371900329
gwascentral	rs371900329
openSNP	rs371900329
23andMe	rs371900329
SNPshot	rs371900329
SNPdbe	rs371900329
MSV3d	rs371900329
GWAS Ctlg	rs371900329

Max Magnitude

0

ClinVar
Risk	rs371900329(T;T)
Alt	rs371900329(T;T)
Reference	Rs371900329(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CALHM1
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.105218048C>T
CLNSRC
CLNACC	RCV000424150.1,