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rs869312940

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312940(A;A)
Make rs869312940(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position88210926
GeneSRI
is asnp
is mentioned by
dbSNPrs869312940
ebirs869312940
HLIrs869312940
Exacrs869312940
Varsomers869312940
Maprs869312940
PheGenIrs869312940
hapmaprs869312940
1000 genomesrs869312940
hgdprs869312940
ensemblrs869312940
gopubmedrs869312940
geneviewrs869312940
scholarrs869312940
googlers869312940
pharmgkbrs869312940
gwascentralrs869312940
openSNPrs869312940
23andMers869312940
23andMe allrs869312940
SNP Nexus

SNPshotrs869312940
SNPdbers869312940
MSV3drs869312940
GWAS Ctlgrs869312940
Max Magnitude0
ClinVar
Risk rs869312940(A;A)
Alt rs869312940(A;A)
Reference rs869312940(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SRI
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000007.13:g.87840241C>T
CLNSRC
CLNACC RCV000210688.1,