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Items: 1 to 100 of 108

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr12:112856920
GRCh38:
Chr12:112419116
PTPN11Noonan syndrome 1, Noonan syndrome, not provided
Pathogenic
(Feb 10, 2016)
criteria provided, multiple submitters, no conflicts
2.
GRCh37:
Chr12:112884113
GRCh38:
Chr12:112446309
PTPN11Metachondromatosis, Noonan syndrome with multiple lentigines, Noonan syndrome,
not specified
Conflicting interpretations of pathogenicity
(Jun 14, 2016)
criteria provided, conflicting interpretations
3.
GRCh37:
Chr12:112884131
GRCh38:
Chr12:112446327
PTPN11not specifiedLikely benign
(Mar 1, 2008)
criteria provided, single submitter
4.
GRCh37:
Chr12:112884184
GRCh38:
Chr12:112446380
PTPN11not specifiedUncertain significance
(Oct 1, 2012)
criteria provided, single submitter
5.
GRCh37:
Chr12:112884189
GRCh38:
Chr12:112446385
PTPN11Noonan syndrome, not provided, Rasopathy
Pathogenic
(Jun 23, 2016)
criteria provided, multiple submitters, no conflicts
6.
GRCh37:
Chr12:112888139
GRCh38:
Chr12:112450335
PTPN11Noonan syndrome, not providedLikely pathogenic
(Nov 18, 2014)
criteria provided, multiple submitters, no conflicts
7.
GRCh37:
Chr12:112888150
GRCh38:
Chr12:112450346
PTPN11not specifiedUncertain significance
(Sep 25, 2013)
criteria provided, multiple submitters, no conflicts
8.
GRCh37:
Chr12:112888156
GRCh38:
Chr12:112450352
PTPN11Noonan syndrome, not provided, Rasopathy
Pathogenic
(Jan 18, 2017)
criteria provided, multiple submitters, no conflicts
9.
GRCh37:
Chr12:112888156
GRCh38:
Chr12:112450352
PTPN11Noonan syndrome 1, Noonan syndrome, not provided,
Rasopathy
Pathogenic
(Dec 5, 2016)
criteria provided, multiple submitters, no conflicts
10.
GRCh37:
Chr12:112888158
GRCh38:
Chr12:112450354
PTPN11Noonan syndrome 1, Juvenile myelomonocytic leukemia, Metachondromatosis,
LEOPARD syndrome 1, Noonan syndrome, not provided
Pathogenic/Likely pathogenic
(May 18, 2017)
criteria provided, multiple submitters, no conflicts
11.
GRCh37:
Chr12:112888158
GRCh38:
Chr12:112450354
PTPN11Noonan syndrome, not providedPathogenic
(Apr 6, 2017)
criteria provided, multiple submitters, no conflicts
12.
GRCh37:
Chr12:112888162
GRCh38:
Chr12:112450358
PTPN11Noonan syndrome, not providedPathogenic/Likely pathogenic
(Jan 15, 2015)
criteria provided, multiple submitters, no conflicts
13.
GRCh37:
Chr12:112888163
GRCh38:
Chr12:112450359
PTPN11Noonan syndrome 1, Noonan syndrome, not provided,
Rasopathy
Pathogenic
(Dec 24, 2016)
criteria provided, multiple submitters, no conflicts
14.
GRCh37:
Chr12:112888165
GRCh38:
Chr12:112450361
PTPN11Juvenile myelomonocytic leukemiaPathogenic
(Feb 6, 2015)
criteria provided, single submitter
15.
GRCh37:
Chr12:112888165
GRCh38:
Chr12:112450361
PTPN11not provided, RasopathyPathogenic
(May 11, 2017)
criteria provided, multiple submitters, no conflicts
16.
GRCh37:
Chr12:112888166
GRCh38:
Chr12:112450362
PTPN11Noonan syndromeLikely pathogenic
(Aug 9, 2013)
criteria provided, single submitter
17.
GRCh37:
Chr12:112888166
GRCh38:
Chr12:112450362
PTPN11Noonan syndrome 1, Noonan syndrome, not provided,
Rasopathy
Pathogenic
(Feb 3, 2017)
criteria provided, multiple submitters, no conflicts
18.
GRCh37:
Chr12:112888168
GRCh38:
Chr12:112450364
PTPN11Noonan syndrome 1, Noonan syndrome, not provided,
Rasopathy
Pathogenic
(Feb 3, 2017)
criteria provided, multiple submitters, no conflicts
19.
GRCh37:
Chr12:112888172
GRCh38:
Chr12:112450368
PTPN11Noonan syndrome 1, Juvenile myelomonocytic leukemia, Metachondromatosis,
LEOPARD syndrome 1, Noonan syndrome, not provided,
Rasopathy
Pathogenic
(May 18, 2017)
criteria provided, multiple submitters, no conflicts
20.
GRCh37:
Chr12:112888189
GRCh38:
Chr12:112450385
PTPN11Noonan syndrome, not provided, Rasopathy
Pathogenic
(Aug 12, 2016)
criteria provided, multiple submitters, no conflicts
21.
GRCh37:
Chr12:112888190
GRCh38:
Chr12:112450386
PTPN11not specifiedUncertain significance
(Mar 1, 2008)
criteria provided, single submitter
22.
GRCh37:
Chr12:112888193
GRCh38:
Chr12:112450389
PTPN11Noonan syndrome, not provided, Rasopathy
Pathogenic/Likely pathogenic
(Feb 3, 2017)
criteria provided, multiple submitters, no conflicts
23.
GRCh37:
Chr12:112888195
GRCh38:
Chr12:112450391
PTPN11Noonan syndrome, not providedPathogenic/Likely pathogenic
(Mar 22, 2017)
criteria provided, multiple submitters, no conflicts
24.
GRCh37:
Chr12:112888198
GRCh38:
Chr12:112450394
PTPN11Chronic lymphocytic leukemia, Neuroblastoma, Acute myeloid leukemia,
Rasopathy, Neoplasm of brain
Likely pathogenic
(May 31, 2016)
criteria provided, single submitter
25.
GRCh37:
Chr12:112888198
GRCh38:
Chr12:112450394
PTPN11Noonan syndrome, not providedPathogenic/Likely pathogenic
(Feb 4, 2013)
criteria provided, multiple submitters, no conflicts
26.
GRCh37:
Chr12:112888198
GRCh38:
Chr12:112450394
PTPN11Noonan syndrome 1, Noonan syndrome, not provided,
Rasopathy
Pathogenic
(Feb 3, 2017)
criteria provided, multiple submitters, no conflicts
27.
GRCh37:
Chr12:112888199
GRCh38:
Chr12:112450395
PTPN11Noonan syndrome 1, Juvenile myelomonocytic leukemia, Metachondromatosis,
LEOPARD syndrome 1, Noonan syndrome, not provided
Pathogenic
(May 18, 2017)
criteria provided, multiple submitters, no conflicts
28.
GRCh37:
Chr12:112888201-112888202
GRCh38:
Chr12:112450397-112450398
PTPN11Noonan syndromePathogenic
(Apr 2, 2013)
criteria provided, single submitter
29.
GRCh37:
Chr12:112888202
GRCh38:
Chr12:112450398
PTPN11Noonan syndrome 1, Juvenile myelomonocytic leukemia, Metachondromatosis,
LEOPARD syndrome 1, Noonan syndrome, not provided,
Rasopathy
Pathogenic
(May 18, 2017)
criteria provided, multiple submitters, no conflicts
30.
GRCh37:
Chr12:112888211
GRCh38:
Chr12:112450407
PTPN11Multiple myeloma, Neuroblastoma, Juvenile myelomonocytic leukemia,
Squamous cell carcinoma of lung, not provided, Astrocytoma,
Colorectal Neoplasms
Pathogenic/Likely pathogenic
(May 31, 2016)
criteria provided, multiple submitters, no conflicts
31.
GRCh37:
Chr12:112888212
GRCh38:
Chr12:112450408
PTPN11Noonan syndrome, not provided, Rasopathy
Pathogenic
(Jan 2, 2017)
criteria provided, multiple submitters, no conflicts
32.
GRCh37:
Chr12:112888212
GRCh38:
Chr12:112450408
PTPN11Noonan syndrome, not provided, Rasopathy
Pathogenic
(Oct 11, 2016)
criteria provided, multiple submitters, no conflicts
33.
GRCh37:
Chr12:112888219
GRCh38:
Chr12:112450415
PTPN11Noonan syndromeLikely pathogenic
(Jan 28, 2013)
criteria provided, single submitter
34.
GRCh37:
Chr12:112888220
GRCh38:
Chr12:112450416
PTPN11Noonan syndrome 1, Juvenile myelomonocytic leukemia, Metachondromatosis,
LEOPARD syndrome 1, Noonan syndrome, not provided,
Rasopathy
Pathogenic
(May 18, 2017)
criteria provided, multiple submitters, no conflicts
35.
GRCh37:
Chr12:112888239
GRCh38:
Chr12:112450435
PTPN11Metachondromatosis, Noonan syndrome with multiple lentigines, Noonan syndrome,
not specified, Rasopathy, Cardiovascular phenotype
Benign/Likely benign
(Apr 14, 2017)
criteria provided, multiple submitters, no conflicts
36.
GRCh37:
Chr12:112888299
GRCh38:
Chr12:112450495
PTPN11not specifiedLikely benign
(May 17, 2012)
criteria provided, single submitter
37.
GRCh37:
Chr12:112888301
GRCh38:
Chr12:112450497
PTPN11Noonan syndrome, not provided, Rasopathy
Pathogenic
(May 13, 2016)
criteria provided, multiple submitters, no conflicts
38.
GRCh37:
Chr12:112888312
GRCh38:
Chr12:112450508
PTPN11Noonan syndrome, not providedPathogenic
(Mar 8, 2016)
criteria provided, multiple submitters, no conflicts
39.
GRCh37:
Chr12:112890996
GRCh38:
Chr12:112453192
PTPN11not specified, RasopathyConflicting interpretations of pathogenicity
(May 6, 2015)
criteria provided, conflicting interpretations
40.
GRCh37:
Chr12:112891058
GRCh38:
Chr12:112453254
PTPN11not specifiedConflicting interpretations of pathogenicity
(May 10, 2016)
criteria provided, conflicting interpretations
41.
GRCh37:
Chr12:112891083
GRCh38:
Chr12:112453279
PTPN11Noonan syndrome 1, Juvenile myelomonocytic leukemia, Metachondromatosis,
LEOPARD syndrome 1, not specified, not provided,
Rasopathy
Pathogenic
(May 18, 2017)
criteria provided, multiple submitters, no conflicts
42.
GRCh37:
Chr12:112891083
GRCh38:
Chr12:112453279
PTPN11not provided, RasopathyPathogenic
(Oct 10, 2016)
criteria provided, multiple submitters, no conflicts
43.
GRCh37:
Chr12:112891203
GRCh38:
Chr12:112453399
PTPN11Noonan syndrome, not specifiedBenign
(Oct 19, 2016)
criteria provided, multiple submitters, no conflicts
44.
GRCh37:
Chr12:112892360
GRCh38:
Chr12:112454556
PTPN11Noonan syndrome, not specified, not provided,
Rasopathy
Benign/Likely benign
(Oct 17, 2016)
criteria provided, multiple submitters, no conflicts
45.
GRCh37:
Chr12:112892398
GRCh38:
Chr12:112454594
PTPN11Noonan syndrome, not specifiedUncertain significance
(Dec 12, 2011)
criteria provided, single submitter
46.
GRCh37:
Chr12:112892400
GRCh38:
Chr12:112454596
PTPN11not specifiedBenign/Likely benign
(Jul 28, 2015)
criteria provided, multiple submitters, no conflicts
47.
GRCh37:
Chr12:112892440
GRCh38:
Chr12:112454636
PTPN11Noonan syndrome, not providedPathogenic/Likely pathogenic
(Apr 26, 2016)
criteria provided, multiple submitters, no conflicts
48.
GRCh37:
Chr12:112893772
GRCh38:
Chr12:112455968
PTPN11MetachondromatosisPathogenic
(Sep 7, 2011)
criteria provided, single submitter
49.
GRCh37:
Chr12:112893772
GRCh38:
Chr12:112455968
PTPN11not specifiedUncertain significance
(Dec 12, 2012)
criteria provided, single submitter
50.
GRCh37:
Chr12:112910758
GRCh38:
Chr12:112472954
PTPN11not specified, not provided, Rasopathy
Pathogenic/Likely pathogenic
(Jun 13, 2017)
criteria provided, multiple submitters, no conflicts
51.
GRCh37:
Chr12:112910765
GRCh38:
Chr12:112472961
PTPN11Noonan syndrome, not providedPathogenic/Likely pathogenic
(Sep 29, 2015)
criteria provided, multiple submitters, no conflicts
52.
GRCh37:
Chr12:112910772
GRCh38:
Chr12:112472968
PTPN11Noonan syndrome, not providedPathogenic/Likely pathogenic
(Oct 26, 2016)
criteria provided, multiple submitters, no conflicts
53.
GRCh37:
Chr12:112910785
GRCh38:
Chr12:112472981
PTPN11Noonan syndrome 1, Noonan syndrome, not specified,
not provided, Rasopathy
Conflicting interpretations of pathogenicity
(Feb 3, 2017)
criteria provided, conflicting interpretations
54.
GRCh37:
Chr12:112910793
GRCh38:
Chr12:112472989
PTPN11Noonan syndrome, not providedLikely pathogenic
(Nov 21, 2016)
criteria provided, multiple submitters, no conflicts
55.
GRCh37:
Chr12:112910793
GRCh38:
Chr12:112472989
PTPN11Noonan syndrome, not providedPathogenic/Likely pathogenic
(Aug 9, 2016)
criteria provided, multiple submitters, no conflicts
56.
GRCh37:
Chr12:112910822
GRCh38:
Chr12:112473018
PTPN11not specifiedLikely benign
(Sep 28, 2015)
criteria provided, single submitter
57.
GRCh37:
Chr12:112910827
GRCh38:
Chr12:112473023
PTPN11LEOPARD syndrome 1, Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia, Noonan syndrome,
not provided, Rasopathy
Pathogenic
(Dec 27, 2016)
criteria provided, multiple submitters, no conflicts
58.
GRCh37:
Chr12:112910835
GRCh38:
Chr12:112473031
PTPN11Noonan syndrome 1, not provided, Rasopathy
Pathogenic
(Dec 21, 2016)
criteria provided, multiple submitters, no conflicts
59.
GRCh37:
Chr12:112910837
GRCh38:
Chr12:112473033
PTPN11Noonan syndrome, not providedPathogenic/Likely pathogenic
(Apr 7, 2016)
criteria provided, multiple submitters, no conflicts
60.
GRCh37:
Chr12:112910844
GRCh38:
Chr12:112473040
PTPN11Noonan syndrome, not provided, Rasopathy
Pathogenic
(Feb 2, 2017)
criteria provided, multiple submitters, no conflicts
61.
GRCh37:
Chr12:112915455
GRCh38:
Chr12:112477651
PTPN11Noonan syndrome, not provided, Rasopathy
Pathogenic
(Jun 13, 2015)
criteria provided, multiple submitters, no conflicts
62.
GRCh37:
Chr12:112915455
GRCh38:
Chr12:112477651
PTPN11Noonan syndrome 1, Noonan syndrome, not provided,
Rasopathy, Early T cell progenitor acute lymphoblastic leukemia
Pathogenic
(Feb 2, 2017)
criteria provided, multiple submitters, no conflicts
63.
GRCh37:
Chr12:112915456
GRCh38:
Chr12:112477652
PTPN11Noonan syndrome, not providedPathogenic
(Feb 2, 2017)
criteria provided, multiple submitters, no conflicts
64.
GRCh37:
Chr12:112915459
GRCh38:
Chr12:112477655
PTPN11not specifiedUncertain significance
(Nov 10, 2014)
criteria provided, single submitter
65.
GRCh37:
Chr12:112915523
GRCh38:
Chr12:112477719
PTPN11Noonan syndrome 1, Juvenile myelomonocytic leukemia, Metachondromatosis,
LEOPARD syndrome 1, Noonan syndrome, not specified,
not provided, Rasopathy
Pathogenic
(May 31, 2017)
criteria provided, multiple submitters, no conflicts
66.
GRCh37:
Chr12:112915524
GRCh38:
Chr12:112477720
PTPN11Noonan syndrome, not providedPathogenic
(Nov 4, 2016)
criteria provided, multiple submitters, no conflicts
67.
GRCh37:
Chr12:112915524
GRCh38:
Chr12:112477720
PTPN11Noonan syndrome 1, Juvenile myelomonocytic leukemia, Metachondromatosis,
LEOPARD syndrome 1, Noonan syndrome, not specified,
not provided, Rasopathy
Pathogenic
(May 18, 2017)
criteria provided, multiple submitters, no conflicts
68.
GRCh37:
Chr12:112915526
GRCh38:
Chr12:112477722
PTPN11not specified, Rasopathy, Cardiovascular phenotype
Conflicting interpretations of pathogenicity
(Sep 26, 2016)
criteria provided, conflicting interpretations
69.
GRCh37:
Chr12:112915717
GRCh38:
Chr12:112477913
PTPN11not specified, RasopathyBenign/Likely benign
(Jan 29, 2016)
criteria provided, multiple submitters, no conflicts
70.
GRCh37:
Chr12:112919869
GRCh38:
Chr12:112482065
PTPN11Metachondromatosis, Noonan syndrome with multiple lentigines, Noonan syndrome,
not specified, Rasopathy
Benign/Likely benign
(Jan 18, 2017)
criteria provided, multiple submitters, no conflicts
71.
GRCh37:
Chr12:112919909
GRCh38:
Chr12:112482105
PTPN11not specifiedUncertain significance
(Nov 5, 2010)
criteria provided, single submitter
72.
GRCh37:
Chr12:112919946
GRCh38:
Chr12:112482142
PTPN11not specifiedLikely benign
(Jul 11, 2014)
criteria provided, single submitter
73.
GRCh37:
Chr12:112920024
GRCh38:
Chr12:112482220
PTPN11not specifiedLikely benign
(Jan 19, 2016)
criteria provided, multiple submitters, no conflicts
74.
GRCh37:
Chr12:112924272
GRCh38:
Chr12:112486468
PTPN11not specifiedUncertain significance
(Mar 3, 2010)
criteria provided, single submitter
75.
GRCh37:
Chr12:112924280
GRCh38:
Chr12:112486476
PTPN11not specifiedUncertain significance
(Feb 20, 2016)
criteria provided, multiple submitters, no conflicts
76.
GRCh37:
Chr12:112924420
GRCh38:
Chr12:112486616
PTPN11not specified, RasopathyUncertain significance
(Jun 28, 2016)
criteria provided, multiple submitters, no conflicts
77.
GRCh37:
Chr12:112924428
GRCh38:
Chr12:112486624
PTPN11not specifiedUncertain significance
(Feb 2, 2010)
criteria provided, single submitter
78.
GRCh37:
Chr12:112926243
GRCh38:
Chr12:112488439
PTPN11not specifiedLikely benign
(Sep 9, 2015)
criteria provided, single submitter
79.
GRCh37:
Chr12:112926248
GRCh38:
Chr12:112488444
PTPN11Noonan syndrome with multiple lentigines, not providedPathogenic
(Feb 8, 2014)
criteria provided, multiple submitters, no conflicts
80.
GRCh37:
Chr12:112926248
GRCh38:
Chr12:112488444
PTPN11Noonan syndrome with multiple lentigines, LEOPARD syndrome 1, not provided
Pathogenic
(Feb 26, 2015)
criteria provided, multiple submitters, no conflicts
81.
GRCh37:
Chr12:112926258
GRCh38:
Chr12:112488454
PTPN11LEOPARD syndrome 1, not provided, Rasopathy
Pathogenic
(May 10, 2017)
criteria provided, multiple submitters, no conflicts
82.
GRCh37:
Chr12:112926270
GRCh38:
Chr12:112488466
PTPN11Noonan syndrome 1, Juvenile myelomonocytic leukemia, Metachondromatosis,
Noonan syndrome with multiple lentigines, LEOPARD syndrome 1, Noonan syndrome,
not specified, not provided, Rasopathy,
Cardiovascular phenotype
Pathogenic/Likely pathogenic
(Jun 21, 2017)
criteria provided, multiple submitters, no conflicts
83.
GRCh37:
Chr12:112926829
GRCh38:
Chr12:112489025
PTPN11Metachondromatosis, Noonan syndrome with multiple lentigines, Noonan syndrome,
not specified
Conflicting interpretations of pathogenicity
(Jun 14, 2016)
criteria provided, conflicting interpretations
84.
GRCh37:
Chr12:112926851
GRCh38:
Chr12:112489047
PTPN11Noonan syndrome, not provided, Rasopathy
Pathogenic
(Feb 2, 2017)
criteria provided, multiple submitters, no conflicts
85.
GRCh37:
Chr12:112926851
GRCh38:
Chr12:112489047
PTPN11Noonan syndrome, not providedPathogenic
(Sep 11, 2015)
criteria provided, multiple submitters, no conflicts
86.
GRCh37:
Chr12:112926852
GRCh38:
Chr12:112489048
PTPN11Noonan syndrome, not provided, Rasopathy
Pathogenic
(Feb 3, 2017)
criteria provided, multiple submitters, no conflicts
87.
GRCh37:
Chr12:112926852
GRCh38:
Chr12:112489048
PTPN11Noonan syndrome, not providedPathogenic
(May 17, 2017)
criteria provided, multiple submitters, no conflicts
88.
GRCh37:
Chr12:112926872
GRCh38:
Chr12:112489068
PTPN11LEOPARD syndrome 1, not provided, Rasopathy
Pathogenic
(Jan 5, 2017)
criteria provided, multiple submitters, no conflicts
89.
GRCh37:
Chr12:112926873
GRCh38:
Chr12:112489069
PTPN11Noonan syndrome 1, LEOPARD syndrome 1, not provided,
Rasopathy
Pathogenic
(Sep 28, 2016)
criteria provided, multiple submitters, no conflicts
90.
GRCh37:
Chr12:112926882
GRCh38:
Chr12:112489078
PTPN11Noonan syndrome, not provided, Rasopathy
Pathogenic
(Dec 25, 2016)
criteria provided, multiple submitters, no conflicts
91.
GRCh37:
Chr12:112926884
GRCh38:
Chr12:112489080
PTPN11not provided, RasopathyPathogenic
(Feb 1, 2017)
criteria provided, multiple submitters, no conflicts
92.
GRCh37:
Chr12:112926884
GRCh38:
Chr12:112489080
PTPN11Noonan syndrome 1, Noonan syndrome, not provided,
Rasopathy
Pathogenic
(Dec 5, 2016)
criteria provided, multiple submitters, no conflicts
93.
GRCh37:
Chr12:112926885
GRCh38:
Chr12:112489081
PTPN11Noonan syndrome, not providedPathogenic
(Jun 25, 2015)
criteria provided, multiple submitters, no conflicts
94.
GRCh37:
Chr12:112926887
GRCh38:
Chr12:112489083
PTPN11Noonan syndrome, not provided, Rasopathy
Pathogenic
(Jun 12, 2017)
criteria provided, multiple submitters, no conflicts
95.
GRCh37:
Chr12:112926887
GRCh38:
Chr12:112489083
PTPN11Noonan syndrome 1, Juvenile myelomonocytic leukemia, Metachondromatosis,
LEOPARD syndrome 1, Noonan syndrome, not provided,
Rasopathy
Pathogenic
(May 18, 2017)
criteria provided, multiple submitters, no conflicts
96.
GRCh37:
Chr12:112926890
GRCh38:
Chr12:112489086
PTPN11Noonan syndrome, not specified, not provided,
Rasopathy, Cardiovascular phenotype
Pathogenic
(May 22, 2017)
criteria provided, multiple submitters, no conflicts
97.
GRCh37:
Chr12:112926897
GRCh38:
Chr12:112489093
PTPN11Noonan syndrome with multiple lentigines, LEOPARD syndrome 1, not provided,
Rasopathy
Pathogenic
(Sep 13, 2016)
criteria provided, multiple submitters, no conflicts
98.
GRCh37:
Chr12:112926908
GRCh38:
Chr12:112489104
PTPN11LEOPARD syndrome 1, not provided, Rasopathy
Pathogenic
(Feb 3, 2017)
criteria provided, multiple submitters, no conflicts
99.
GRCh37:
Chr12:112926909
GRCh38:
Chr12:112489105
PTPN11LEOPARD syndrome 1, not provided, Rasopathy
Pathogenic
(Dec 19, 2016)
criteria provided, multiple submitters, no conflicts
100.
GRCh37:
Chr12:112926931
GRCh38:
Chr12:112489127
PTPN11not specifiedLikely benign
(Jun 15, 2015)
criteria provided, single submitter
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