S I D E B A R
Format
Items per page
Sort by

Download:

Choose Destination

Search results

Items: 1 to 100 of 241

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr12:40618810
GRCh38:
Chr12:40225008
LRRK2Parkinson disease 8, autosomal dominantLikely benign
(Jun 14, 2016)
criteria provided, single submitter
2.
GRCh37:
Chr12:40618890
GRCh38:
Chr12:40225088
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
3.
GRCh37:
Chr12:40618961
GRCh38:
Chr12:40225159
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
4.
GRCh37:
Chr12:40619082
GRCh38:
Chr12:40225280
LRRK2Parkinson disease 8, autosomal dominant, not specifiedConflicting interpretations of pathogenicity
(Jan 30, 2017)
criteria provided, conflicting interpretations
5.
GRCh37:
Chr12:40619360
GRCh38:
Chr12:40225558
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
6.
GRCh37:
Chr12:40619430
GRCh38:
Chr12:40225628
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
7.
GRCh37:
Chr12:40626182
GRCh38:
Chr12:40232380
LRRK2Parkinson disease 8, autosomal dominantConflicting interpretations of pathogenicity
(Aug 2, 2017)
criteria provided, conflicting interpretations
8.
GRCh37:
Chr12:40629436
GRCh38:
Chr12:40235634
LRRK2Parkinson disease 8, autosomal dominantConflicting interpretations of pathogenicity
(Dec 19, 2016)
criteria provided, conflicting interpretations
9.
GRCh37:
Chr12:40629444
GRCh38:
Chr12:40235642
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
10.
GRCh37:
Chr12:40631791
GRCh38:
Chr12:40237989
LRRK2Parkinson disease 8, autosomal dominantConflicting interpretations of pathogenicity
(Jun 14, 2016)
criteria provided, conflicting interpretations
11.
GRCh37:
Chr12:40631880
GRCh38:
Chr12:40238078
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
12.
GRCh37:
Chr12:40634345
GRCh38:
Chr12:40240543
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
13.
GRCh37:
Chr12:40634396
GRCh38:
Chr12:40240594
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jul 10, 2017)
criteria provided, single submitter
14.
GRCh37:
Chr12:40634404
GRCh38:
Chr12:40240602
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Dec 11, 2014)
no assertion criteria provided
15.
GRCh37:
Chr12:40637357-40637359
GRCh38:
Chr12:40243555-40243557
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
16.
GRCh37:
Chr12:40637358
GRCh38:
Chr12:40243556
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
17.
GRCh37:
Chr12:40637470
GRCh38:
Chr12:40243668
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
18.
GRCh37:
Chr12:40643645
GRCh38:
Chr12:40249843
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Dec 11, 2014)
no assertion criteria provided
19.
GRCh37:
Chr12:40643656
GRCh38:
Chr12:40249854
LRRK2Parkinson disease 8, autosomal dominantLikely benign
(Jun 14, 2016)
criteria provided, single submitter
20.
GRCh37:
Chr12:40643656
GRCh38:
Chr12:40249854
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
21.
GRCh37:
Chr12:40643683
GRCh38:
Chr12:40249881
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
22.
GRCh37:
Chr12:40643725
GRCh38:
Chr12:40249923
LRRK2Parkinson disease 8, autosomal dominantConflicting interpretations of pathogenicity
(Jun 14, 2016)
criteria provided, conflicting interpretations
23.
GRCh37:
Chr12:40645075
GRCh38:
Chr12:40251273
LRRK2Parkinson disease 8, autosomal dominant, not providedConflicting interpretations of pathogenicity
(Jul 31, 2016)
criteria provided, conflicting interpretations
24.
GRCh37:
Chr12:40645163
GRCh38:
Chr12:40251361
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
25.
GRCh37:
Chr12:40645171
GRCh38:
Chr12:40251369
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
26.
GRCh37:
Chr12:40645257
GRCh38:
Chr12:40251455
LRRK2Parkinson disease 8, autosomal dominantBenign
(Jun 14, 2016)
criteria provided, single submitter
27.
GRCh37:
Chr12:40645297
GRCh38:
Chr12:40251495
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Dec 11, 2014)
no assertion criteria provided
28.
GRCh37:
Chr12:40646708
GRCh38:
Chr12:40252906
LRRK2Parkinson disease 8, autosomal dominantBenign/Likely benign
(Jul 14, 2017)
criteria provided, multiple submitters, no conflicts
29.
GRCh37:
Chr12:40646731
GRCh38:
Chr12:40252929
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jul 14, 2017)
criteria provided, single submitter
30.
GRCh37:
Chr12:40646776
GRCh38:
Chr12:40252974
LRRK2not providedLikely pathogenic
(Oct 30, 2017)
criteria provided, single submitter
31.
GRCh37:
Chr12:40646780
GRCh38:
Chr12:40252978
LRRK2not providedUncertain significance
(Jul 31, 2016)
criteria provided, single submitter
32.
GRCh37:
Chr12:40646786
GRCh38:
Chr12:40252984
LRRK2Parkinson disease 8, autosomal dominantPathogenic
(Sep 13, 2012)
no assertion criteria provided
33.
GRCh37:
Chr12:40646818
GRCh38:
Chr12:40253016
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Dec 11, 2014)
no assertion criteria provided
34.
GRCh37:
Chr12:40651144
GRCh38:
Chr12:40257342
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
35.
GRCh37:
Chr12:40653309
GRCh38:
Chr12:40259507
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
36.
GRCh37:
Chr12:40653327
GRCh38:
Chr12:40259525
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
37.
GRCh37:
Chr12:40653380
GRCh38:
Chr12:40259578
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
38.
GRCh37:
Chr12:40657608
GRCh38:
Chr12:40263806
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
39.
GRCh37:
Chr12:40657677
GRCh38:
Chr12:40263875
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
40.
GRCh37:
Chr12:40657700
GRCh38:
Chr12:40263898
LRRK2Parkinson disease 8, autosomal dominantConflicting interpretations of pathogenicity
(Jun 14, 2016)
criteria provided, conflicting interpretations
41.
GRCh37:
Chr12:40668402
GRCh38:
Chr12:40274600
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
42.
GRCh37:
Chr12:40668683
GRCh38:
Chr12:40274881
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Dec 11, 2014)
no assertion criteria provided
43.
GRCh37:
Chr12:40668701
GRCh38:
Chr12:40274899
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
44.
GRCh37:
Chr12:40671735
GRCh38:
Chr12:40277933
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
45.
GRCh37:
Chr12:40671770
GRCh38:
Chr12:40277968
LRRK2Parkinson disease 8, autosomal dominant, not specifiedConflicting interpretations of pathogenicity
(Jan 27, 2017)
criteria provided, conflicting interpretations
46.
GRCh37:
Chr12:40671827
GRCh38:
Chr12:40278025
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
47.
GRCh37:
Chr12:40671956
GRCh38:
Chr12:40278154
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
48.
GRCh37:
Chr12:40671969
GRCh38:
Chr12:40278167
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
49.
GRCh37:
Chr12:40671989
GRCh38:
Chr12:40278187
LRRK2Parkinson disease 8, autosomal dominantConflicting interpretations of pathogenicity
(Jun 14, 2016)
criteria provided, conflicting interpretations
50.
GRCh37:
Chr12:40677699
GRCh38:
Chr12:40283897
LRRK2Parkinson disease 8, autosomal dominantConflicting interpretations of pathogenicity
(Jun 14, 2016)
criteria provided, conflicting interpretations
51.
GRCh37:
Chr12:40677749
GRCh38:
Chr12:40283947
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Dec 11, 2014)
no assertion criteria provided
52.
GRCh37:
Chr12:40677787
GRCh38:
Chr12:40283985
LRRK2Parkinson disease, late-onsetUncertain significance
(Jan 22, 2014)
no assertion criteria provided
53.
GRCh37:
Chr12:40677813
GRCh38:
Chr12:40284011
LRRK2Parkinson disease 8, autosomal dominantConflicting interpretations of pathogenicity
(Jun 14, 2016)
criteria provided, conflicting interpretations
54.
GRCh37:
Chr12:40677863
GRCh38:
Chr12:40284061
LRRK2Parkinson disease 8, autosomal dominant, not specifiedUncertain significance
(Mar 15, 2017)
criteria provided, single submitter
55.
GRCh37:
Chr12:40677916
GRCh38:
Chr12:40284114
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
56.
GRCh37:
Chr12:40681144-40681145
GRCh38:
Chr12:40287342-40287343
LRRK2not specifiedBenign
(Jul 13, 2017)
criteria provided, single submitter
57.
GRCh37:
Chr12:40681144
GRCh38:
Chr12:40287342
LRRK2Parkinson disease 8, autosomal dominantBenign
(Jun 14, 2016)
criteria provided, single submitter
58.
GRCh37:
Chr12:40681240
GRCh38:
Chr12:40287438
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
59.
GRCh37:
Chr12:40681263
GRCh38:
Chr12:40287461
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
60.
GRCh37:
Chr12:40681361
GRCh38:
Chr12:40287559
LRRK2Parkinson disease 8, autosomal dominantLikely benign
(Jun 14, 2016)
criteria provided, single submitter
61.
GRCh37:
Chr12:40687358-40687359
GRCh38:
Chr12:40293556-40293557
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 27, 2017)
criteria provided, single submitter
62.
GRCh37:
Chr12:40687426
GRCh38:
Chr12:40293624
LRRK2Parkinson disease 8, autosomal dominant, not specifiedUncertain significance
(Mar 1, 2017)
criteria provided, single submitter
63.
GRCh37:
Chr12:40687446
GRCh38:
Chr12:40293644
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
64.
GRCh37:
Chr12:40688664
GRCh38:
Chr12:40294862
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
65.
GRCh37:
Chr12:40688668
GRCh38:
Chr12:40294866
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
66.
GRCh37:
Chr12:40688695
GRCh38:
Chr12:40294893
LRRK2Parkinson disease 8, autosomal dominantConflicting interpretations of pathogenicity
(Jun 14, 2016)
criteria provided, conflicting interpretations
67.
GRCh37:
Chr12:40689250
GRCh38:
Chr12:40295448
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
68.
GRCh37:
Chr12:40689268
GRCh38:
Chr12:40295466
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
69.
GRCh37:
Chr12:40689337
GRCh38:
Chr12:40295535
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
70.
GRCh37:
Chr12:40689368
GRCh38:
Chr12:40295566
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
71.
GRCh37:
Chr12:40689371
GRCh38:
Chr12:40295569
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
72.
GRCh37:
Chr12:40689376
GRCh38:
Chr12:40295574
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
73.
GRCh37:
Chr12:40692135
GRCh38:
Chr12:40298333
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Dec 11, 2014)
no assertion criteria provided
74.
GRCh37:
Chr12:40692148
GRCh38:
Chr12:40298346
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
75.
GRCh37:
Chr12:40692235
GRCh38:
Chr12:40298433
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
76.
GRCh37:
Chr12:40692281
GRCh38:
Chr12:40298479
LRRK2Parkinson disease 8, autosomal dominantConflicting interpretations of pathogenicity
(Jun 14, 2016)
criteria provided, conflicting interpretations
77.
GRCh37:
Chr12:40692290
GRCh38:
Chr12:40298488
LRRK2Parkinson disease 8, autosomal dominantPathogenic
(Sep 13, 2012)
no assertion criteria provided
78.
GRCh37:
Chr12:40692927
GRCh38:
Chr12:40299125
LRRK2Parkinson disease 8, autosomal dominantPathogenic
(Sep 13, 2012)
no assertion criteria provided
79.
GRCh37:
Chr12:40692992
GRCh38:
Chr12:40299190
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
80.
GRCh37:
Chr12:40692998
GRCh38:
Chr12:40299196
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
81.
GRCh37:
Chr12:40693014
GRCh38:
Chr12:40299212
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Dec 19, 2016)
criteria provided, single submitter
82.
GRCh37:
Chr12:40693057
GRCh38:
Chr12:40299255
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
83.
GRCh37:
Chr12:40696583
GRCh38:
Chr12:40302781
LRRK2Parkinson disease 8, autosomal dominantLikely benign
(Jun 14, 2016)
criteria provided, single submitter
84.
GRCh37:
Chr12:40696668
GRCh38:
Chr12:40302866
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
85.
GRCh37:
Chr12:40697754
GRCh38:
Chr12:40303952
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
86.
GRCh37:
Chr12:40697802
GRCh38:
Chr12:40304000
LRRK2Parkinson disease 8, autosomal dominant, not providedUncertain significance
(Jul 19, 2017)
criteria provided, multiple submitters, no conflicts
87.
GRCh37:
Chr12:40697806
GRCh38:
Chr12:40304004
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
88.
GRCh37:
Chr12:40697837
GRCh38:
Chr12:40304035
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
89.
GRCh37:
Chr12:40697842
GRCh38:
Chr12:40304040
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
90.
GRCh37:
Chr12:40697842
GRCh38:
Chr12:40304040
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
91.
GRCh37:
Chr12:40697943
GRCh38:
Chr12:40304141
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
92.
GRCh37:
Chr12:40699578
GRCh38:
Chr12:40305776
LRRK2Parkinson disease 8, autosomal dominantLikely benign
(Jun 14, 2016)
criteria provided, single submitter
93.
GRCh37:
Chr12:40699593
GRCh38:
Chr12:40305791
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
94.
GRCh37:
Chr12:40699673
GRCh38:
Chr12:40305871
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
95.
GRCh37:
Chr12:40702269
GRCh38:
Chr12:40308467
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
96.
GRCh37:
Chr12:40702278
GRCh38:
Chr12:40308476
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
97.
GRCh37:
Chr12:40702283
GRCh38:
Chr12:40308481
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
98.
GRCh37:
Chr12:40702420
GRCh38:
Chr12:40308618
LRRK2Parkinson disease 8, autosomal dominantConflicting interpretations of pathogenicity
(Jun 14, 2016)
criteria provided, conflicting interpretations
99.
GRCh37:
Chr12:40702434
GRCh38:
Chr12:40308632
LRRK2Parkinson disease 8, autosomal dominantUncertain significance
(Sep 13, 2012)
no assertion criteria provided
100.
GRCh37:
Chr12:40702911
GRCh38:
Chr12:40309109
LRRK2Parkinson disease 8, autosomal dominantConflicting interpretations of pathogenicity
(Jun 14, 2016)
criteria provided, conflicting interpretations
Format
Items per page
Sort by

Download:

Choose Destination
Support Center