95524940
3:46902542
3:46902542
C
A/C
Not specified
Not specified
-
SNP
dbSNP
Frequency~Cited~Phenotype_or_Disease
pathogenic
missense variant
T/P
410
410
1
deleterious
0
1001
probably damaging
1
29001
likely benign
29
631
likely disease causing
63
341
tolerated
34
964
high
963
ENST00000313049.9

Creators
Not specifiedSubmitter
Views: 156
Created: 16th Jun 2021 at 11:05
Last updated: 16th Jun 2021 at 11:21

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