rs786205835

Orientation

plus

Stabilized

plus

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

Make rs786205835(A;A)

Make rs786205835(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

19

Position

35039116

Gene	HPN, SCN1B

is a	snp
is	mentioned by
dbSNP	rs786205835
dbSNP (classic)	rs786205835
ClinGen	rs786205835
ebi	rs786205835
HLI	rs786205835
Exac	rs786205835
Gnomad	rs786205835
Varsome	rs786205835
LitVar	rs786205835
Map	rs786205835
PheGenI	rs786205835
Biobank	rs786205835
1000 genomes	rs786205835
hgdp	rs786205835
ensembl	rs786205835
geneview	rs786205835
scholar	rs786205835
google	rs786205835
pharmgkb	rs786205835
gwascentral	rs786205835
openSNP	rs786205835
23andMe	rs786205835
SNPshot	rs786205835
SNPdbe	rs786205835
MSV3d	rs786205835
GWAS Ctlg	rs786205835

Max Magnitude

0

ClinVar
Risk	rs786205835(A;A)
Alt	rs786205835(A;A)
Reference	Rs786205835(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN1B HPN
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.35530020G>A
CLNSRC
CLNACC	RCV000171051.2,