Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11961407
rs11961407
CCHCR1
6 31154630 missense variant G/A snv 3.0E-03 1.3E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2020 2020
dbSNP: rs1214959853
rs1214959853
CCHCR1
6 31150504 missense variant T/C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2004 2004
dbSNP: rs2027937
rs2027937
CCHCR1
6 31148725 missense variant C/T snv 8.3E-02 6.6E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 < 0.001 1 2010 2010