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rs797044954

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044954(A;A)
Make rs797044954(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position75540155
GeneTMEM231
is asnp
is mentioned by
dbSNPrs797044954
ebirs797044954
HLIrs797044954
Exacrs797044954
Varsomers797044954
Maprs797044954
PheGenIrs797044954
hapmaprs797044954
1000 genomesrs797044954
hgdprs797044954
ensemblrs797044954
gopubmedrs797044954
geneviewrs797044954
scholarrs797044954
googlers797044954
pharmgkbrs797044954
gwascentralrs797044954
openSNPrs797044954
23andMers797044954
23andMe allrs797044954
SNP Nexus

SNPshotrs797044954
SNPdbers797044954
MSV3drs797044954
GWAS Ctlgrs797044954
Max Magnitude0
ClinVar
Risk rs797044954(A;A)
Alt rs797044954(A;A)
Reference rs797044954(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene TMEM231
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000016.9:g.75574053C>T
CLNSRC
CLNACC RCV000190811.1,