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

rs775196743

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775196743(A;A)
Make rs775196743(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position104080649
GeneCOL17A1
is asnp
is mentioned by
dbSNPrs775196743
dbSNP (classic)rs775196743
ClinGenrs775196743
ebirs775196743
HLIrs775196743
Exacrs775196743
Gnomadrs775196743
Varsomers775196743
LitVarrs775196743
Maprs775196743
PheGenIrs775196743
Biobankrs775196743
1000 genomesrs775196743
hgdprs775196743
ensemblrs775196743
geneviewrs775196743
scholarrs775196743
googlers775196743
pharmgkbrs775196743
gwascentralrs775196743
openSNPrs775196743
23andMers775196743
SNPshotrs775196743
SNPdbers775196743
MSV3drs775196743
GWAS Ctlgrs775196743
Max Magnitude0
ClinVar
Risk rs775196743(A;A)
Alt rs775196743(A;A)
Reference Rs775196743(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL17A1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.105840407G>A
CLNSRC
CLNACC RCV000489975.1,