rs786205634

Orientation

minus

Stabilized

minus

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

Make rs786205634(-;-)

Make rs786205634(-;A)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

85663648

Gene

SFTPB

is a	snp
is	mentioned by
dbSNP	rs786205634
dbSNP (classic)	rs786205634
ClinGen	rs786205634
ebi	rs786205634
HLI	rs786205634
Exac	rs786205634
Gnomad	rs786205634
Varsome	rs786205634
LitVar	rs786205634
Map	rs786205634
PheGenI	rs786205634
Biobank	rs786205634
1000 genomes	rs786205634
hgdp	rs786205634
ensembl	rs786205634
geneview	rs786205634
scholar	rs786205634
google	rs786205634
pharmgkb	rs786205634
gwascentral	rs786205634
openSNP	rs786205634
23andMe	rs786205634
SNPshot	rs786205634
SNPdbe	rs786205634
MSV3d	rs786205634
GWAS Ctlg	rs786205634

Max Magnitude

0

ClinVar
Risk	rs786205634(-;-)
Alt	rs786205634(-;-)
Reference	Rs786205634(A;A)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	SFTPB
CLNDBN	not specified
Reversed	1
HGVS	NC_000002.11:g.85890771delT
CLNSRC
CLNACC	RCV000171496.2,