chr11:71437944:C>G Detail (hg38) (DHCR7)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
Genome browser

Information

Genome

Assembly	Position
hg19	chr11:71,148,990-71,148,990 View the variant detail on this assembly version.
hg38	chr11:71,437,944-71,437,944

HGVS

DHCR7

Type	Transcript	Protein
RefSeq	NM_001163817.1:c.832-1G>C
	NM_001360.2:c.832-1G>C
Ensemble	ENST00000355527.8:c.832-1G>C
	ENST00000407721.6:c.832-1G>C
	ENST00000526780.6:c.832-1G>C
	ENST00000527316.6:c.658-1G>C
	ENST00000682708.1:c.883-1G>C
	ENST00000682880.1:c.832-1G>C
	ENST00000683287.1:c.868-1G>C
	ENST00000683714.1:c.832-1G>C
	ENST00000685320.1:c.247-1G>C

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic
Review star
Show details

Links

DHCR7

Type	Database	ID	Link
Gene	MIM	602858	OMIM
	HGNC	2860	HGNC
	Ensembl	ENSG00000172893	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2008-04-01	no assertion criteria provided	Smith-Lemli-Opitz syndrome	germline unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.610	Smith-Lemli-Opitz syndrome	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_001360.3(DHCR7):c.832-1G>C AND Smith-Lemli-Opitz syndrome	ClinVar	Detail
NA	DisGeNET	Detail

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs80338863 dbSNP
Genome: hg38
Position: chr11:71,437,944-71,437,944
Variant Type: snv
Reference Allele: C
Alternative Allele: G

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