Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205634

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205634(-;-)
Make rs786205634(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position85663648
GeneSFTPB
is asnp
is mentioned by
dbSNPrs786205634
ebirs786205634
HLIrs786205634
Exacrs786205634
Varsomers786205634
Maprs786205634
PheGenIrs786205634
hapmaprs786205634
1000 genomesrs786205634
hgdprs786205634
ensemblrs786205634
gopubmedrs786205634
geneviewrs786205634
scholarrs786205634
googlers786205634
pharmgkbrs786205634
gwascentralrs786205634
openSNPrs786205634
23andMers786205634
23andMe allrs786205634
SNP Nexus

SNPshotrs786205634
SNPdbers786205634
MSV3drs786205634
GWAS Ctlgrs786205634
Max Magnitude0
ClinVar
Risk rs786205634(;)
Alt rs786205634(;)
Reference rs786205634(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SFTPB
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.85890771delT
CLNSRC
CLNACC RCV000171496.1,