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rs377138881

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377138881(A;A)
Make rs377138881(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position134824666
GeneCOL5A1, LOC101448202
is asnp
is mentioned by
dbSNPrs377138881
ebirs377138881
HLIrs377138881
Exacrs377138881
Varsomers377138881
Maprs377138881
PheGenIrs377138881
hapmaprs377138881
1000 genomesrs377138881
hgdprs377138881
ensemblrs377138881
gopubmedrs377138881
geneviewrs377138881
scholarrs377138881
googlers377138881
pharmgkbrs377138881
gwascentralrs377138881
openSNPrs377138881
23andMers377138881
23andMe allrs377138881
SNP Nexus

SNPshotrs377138881
SNPdbers377138881
MSV3drs377138881
GWAS Ctlgrs377138881
Max Magnitude0
ClinVar
Risk rs377138881(A;A)
Alt rs377138881(A;A)
Reference rs377138881(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL5A1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.137716512G>A
CLNSRC
CLNACC RCV000195865.1,