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Items: 5

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr7:6048973
GRCh38:
Chr7:6009342
PMS2, AIMP2Lynch syndromeBenign
(Sep 5, 2013)
reviewed by expert panel
2.
GRCh37:
Chr7:6048990
GRCh38:
Chr7:6009359
PMS2, AIMP2Lynch syndromeUncertain significance
(Sep 5, 2013)
reviewed by expert panel
3.
GRCh37:
Chr7:6049613
GRCh38:
Chr7:6009982
PMS2, AIMP2Lynch syndromeUncertain significance
(Sep 5, 2013)
reviewed by expert panel
4.
GRCh37:
Chr7:6050796
GRCh38:
Chr7:6011165
PMS2, AIMP2Lynch syndromeBenign
(Sep 5, 2013)
reviewed by expert panel
5.
GRCh37:
Chr7:6051209
GRCh38:
Chr7:6011578
PMS2, AIMP2Lynch syndromeBenign
(Sep 5, 2013)
reviewed by expert panel
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