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Items: 5

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr7:155599203
GRCh38:
Chr7:155806509
SHHHoloprosencephaly 3Pathogenic
(Aug 29, 2013)
no assertion criteria provided
2.
GRCh37:
Chr7:155599203
GRCh38:
Chr7:155806509
SHHHoloprosencephaly 3Pathogenic
(Aug 29, 2013)
no assertion criteria provided
3.
GRCh37:
Chr7:155599239
GRCh38:
Chr7:155806545
SHHHoloprosencephaly 3Pathogenic
(Aug 29, 2013)
no assertion criteria provided
4.
GRCh37:
Chr7:155604519
GRCh38:
Chr7:155811825
SHHHoloprosencephaly 3Pathogenic
(Aug 29, 2013)
no assertion criteria provided
5.
GRCh37:
Chr7:155604726
GRCh38:
Chr7:155812032
SHHHoloprosencephaly 3Pathogenic
(Aug 29, 2013)
no assertion criteria provided
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