Related gene-specific medical variations for Gene (Select 100506495) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 439860	NM_002310.6(LIFR):c.-20+294A>T	LIFR, LIFR-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Stuve-Wiedemann syndrome	GBenign
Select item 353643	NM_002310.6(LIFR):c.-139G>A	LIFR, LIFR-AS1	Single nucleotide variant (5 prime UTR variant)	Stuve-Wiedemann syndrome	GUncertain significance
Select item 353642	NM_002310.6(LIFR):c.-129T>G	LIFR, LIFR-AS1	Single nucleotide variant (5 prime UTR variant)	Stuve-Wiedemann syndrome	GUncertain significance
Select item 353641	NM_002310.6(LIFR):c.-118G>A	LIFR-AS1, LIFR	Single nucleotide variant (5 prime UTR variant)	Stuve-Wiedemann syndrome	GUncertain significance
Select item 353640	NM_002310.6(LIFR):c.-90T>C	LIFR-AS1, LIFR	Single nucleotide variant (5 prime UTR variant)	Stuve-Wiedemann syndrome	GUncertain significance
Select item 353639	NM_002310.6(LIFR):c.-28G>A	LIFR, LIFR-AS1	Single nucleotide variant (5 prime UTR variant)	Stuve-Wiedemann syndrome	GUncertain significance

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