GENETIC ENCYCLOPEDIA
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NM_032193.3(RNASEH2C):c.268_270delAAG AND Aicardi Goutieres syndrome 3

Significance: Benign
ClinVar: RCV000549932

Variant: NM_032193.3(RNASEH2C):c.268_270delAAG

Type: Variant
Allele: NM_032193.3(RNASEH2C):c.268_270delAAG 328506
Gene:
Type: Microsatellite
Location: Chr11: 65487791 - 65487793 - assembly GRCh37
Chr11: 65720320 - 65720322 - assembly GRCh38
References: dbSNP: 141875736
Illumina Clinical Services Laboratory,Illumina: 563495

Condition

Disease: Aicardi Goutieres syndrome 3