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rs768607170

From SNPedia

Orientationplus
Stabilizedplus
Make rs768607170(-;-)
Make rs768607170(-;G)
Make rs768607170(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome10
Position100749771
GenePAX2
is asnp
is mentioned by
dbSNPrs768607170
dbSNP (classic)rs768607170
ClinGenrs768607170
ebirs768607170
HLIrs768607170
Exacrs768607170
Gnomadrs768607170
Varsomers768607170
LitVarrs768607170
Maprs768607170
PheGenIrs768607170
Biobankrs768607170
1000 genomesrs768607170
hgdprs768607170
ensemblrs768607170
geneviewrs768607170
scholarrs768607170
googlers768607170
pharmgkbrs768607170
gwascentralrs768607170
openSNPrs768607170
23andMers768607170
23andMe allrs768607170
SNPshotrs768607170
SNPdbers768607170
MSV3drs768607170
GWAS Ctlgrs768607170
Max Magnitude0

aka NM_003990.4(PAX2):c.76dupG or (p.Val26Glyfs)

OMIM pathogenic variant