95524956
3:46897936
3:46897936
T
C/T
Not specified
Not specified
-
SNP
dbSNP
Frequency~Cited~Phenotype_or_Disease
pathogenic
missense variant
P/L
132
132
1
deleterious
0
1001
probably damaging
1
27001
likely benign
27
886
likely disease causing
885
726
damaging
725
967
high
966
ENST00000313049.9

Creators
Not specifiedSubmitter
Views: 129
Created: 16th Jun 2021 at 11:05

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